Bring your expertise.
Build something that lasts.
Krieger Scientific is building a firm of recognized experts across every discipline required for life sciences compliance. We are not looking for generalists. We are looking for people who have spent their careers developing deep knowledge in their field and want to put that knowledge to work in an environment that values it.
This is a firm being built intentionally. Every role we add strengthens a capability, deepens a practice area, and moves Krieger closer to the kind of organization that the life sciences industry deserves. One where expertise is the standard, not the exception. If that is the kind of place you want to contribute to, we would like to hear from you.
Open Positions
All positions are based in the United States. Candidates must be currently authorized to work in the U.S. on a full-time basis. Krieger Scientific does not sponsor employment visas.
Position: Quality Engineer Consultant
Location: Southern New Jersey (on-site, client locations)
Employment Type: Consulting Engagement
Schedule: 40 hours per week
About the Role
Krieger Scientific has an opportunity for an experienced Quality Engineer Consultant to support a regulated pharmaceutical manufacturing operation in Southern New Jersey. This is a hands-on Quality Engineering role for someone who can work independently within an active manufacturing environment and partner closely with Quality, Manufacturing, Engineering, R&D, Supply Chain, and other technical teams.
The Quality Engineer Consultant will support process validation, equipment qualification, quality investigations, CAPAs, change controls, risk assessments, technical documentation, and manufacturing troubleshooting. The role requires someone who can understand both the
technical and regulatory requirements of a process, ask the right questions, and translate those requirements into clear, compliant execution level documentation.
The initial engagement is expected to run approximately six months with an anticipated October start. As Krieger Scientific continues to grow, this engagement may lead to additional opportunities within the organization.
Key Responsibilities
- Develop and execute validation strategies in accordance with applicable regulatory and customer requirements.
- Author, review, and approve equipment qualification and process validation protocols and reports.
- Define appropriate test cases, acceptance criteria, and validation requirements.
- Coordinate and support protocol execution within the manufacturing environment.
- Evaluate new and modified manufacturing processes against regulatory, customer, and cGMP requirements.
- Support technology transfer and design transfer activities for new or modified products and manufacturing processes.
- Evaluate engineering change controls involving specifications, equipment, processes, and validated systems.
- Lead and support root cause investigations and CAPA activities.
- Author and support process risk assessments.
- Apply statistical and risk-based approaches to manufacturing and Quality issues.
- Identify process improvements that enhance product quality, reduce variation, and improve operational efficiency.
- Work directly with Manufacturing and Engineering to troubleshoot Quality and process issues.
- Author, review, and revise SOPs, specifications, production documentation, validation documentation, and other Quality records.
- Support Material Review Board activities as required.
- Provide Quality direction and technical guidance to cross-functional team members.
- Support customer, supplier, regulatory, and other applicable audits and inspections.
- Identify gaps within existing Quality processes and help develop compliant, practical solutions.
- Manage multiple priorities and projects within a fast-moving manufacturing environment.
Qualifications
- Quality Engineering experience within a regulated pharmaceutical, biotechnology, combination product, or medical device manufacturing environment.
- Strong pharmaceutical manufacturing and cGMP experience preferred.
- Recent hands-on experience with process validation and equipment qualification.
- Experience authoring and executing validation protocols and reports.
- Experience with CAPAs, deviations, nonconformances, change controls, root cause investigations, and risk assessments.
- Understanding of QMS, GxP, and applicable FDA requirements.
- Working knowledge of 21 CFR Parts 210 and 211. Experience with 21 CFR Part 820 and ISO 13485 is a plus.
- Ability to translate regulatory and technical requirements into practical execution level documentation.
- Strong technical writing skills.
- Experience working directly with Manufacturing and Engineering teams in a production environment.
- Ability to independently troubleshoot manufacturing and Quality issues.
- Ability to make sound Quality decisions with limited supervision.
- Strong communication skills and the ability to effectively support Quality requirements across different functional groups.
- Ability to adapt to changing priorities and operate effectively in an evolving manufacturing environment.
- Bachelor’s degree in Engineering, Life Science, Physical Science, or a related technical discipline. Chemical Engineering or a related engineering discipline is preferred.
Preferred Experience
- MasterControl
- Sterile or aseptic manufacturing
- Cleanroom environments
- Purified water or WFI systems
- Extrusion
- Blow fill seal manufacturing
- Container closure integrity testing
- Combination products
- LEAN or Six Sigma training or certification
What Success Looks Like
The successful consultant will be comfortable moving between technical Quality Engineering work and hands on manufacturing support. This person should be able to independently evaluate a process, identify Quality or compliance gaps, determine what documentation or validation work is required, and work collaboratively with technical teams to develop and implement an appropriate solution.
This role is best suited for someone who remains close to the work and is comfortable writing documentation, executing protocols, troubleshooting on the manufacturing floor, and standing behind sound Quality and compliance decisions.
About Krieger Scientific
Krieger Scientific is a full-service compliance and technical solutions firm serving life sciences organizations across the full asset lifecycle. With more than 35 years of industry experience behind its leadership and a proud commitment as a veteran-owned business, Krieger Scientific builds teams around programs and stays focused on what comes next for our clients and for the people who work with us.
Work Authorization
U.S. work authorization required. Visa sponsorship is not available for this position.
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
To Apply
Send your resume to careers@kriegerscientific.com.
Position: Project Lead
Location: Southeastern Pennsylvania (on-site, client locations)
Employment Type: Full-time, Hourly
Schedule: 40 hours per week
About Krieger Scientific
Krieger Scientific is a full-service compliance and technical solutions firm serving life sciences organizations across the full asset lifecycle. With more than 35 years of industry experience behind its leadership and a proud commitment as a veteran-owned business, Krieger Scientific builds teams around programs and stays focused on what comes next for our clients and for the people who work with us.
About the Role
Krieger Scientific is hiring an experienced Project Lead to oversee and support a large-scale calibration program for a life sciences client in the Exton, Pennsylvania area.
This is a full-time, hourly position scheduled for 40 hours per week and is part of a dedicated Krieger Scientific team supporting the client’s calibration program through a staff augmentation engagement.
The Project Lead will serve as the primary onsite lead for the Krieger Scientific team and work closely with client management to organize, prioritize, and support calibration activities across multiple client locations.
This role combines technical calibration knowledge with project leadership, team coordination, client communication, calibration program management, and Continuous Improvement. The Project Lead will provide day-to-day direction to Calibration Technicians while helping maintain an effective, compliant, and sustainable calibration program.
What You Will Do
- Lead the day-to-day execution of the client calibration program across multiple nearby facilities.
- Provide daily direction, priorities, and support to Krieger Scientific Calibration Technicians assigned to the client.
- Work closely with client management to develop and maintain a clear plan for calibration activities, schedules, priorities, and resource requirements.
- Manage calibration schedules and work activities to support timely completion of required calibrations.
- Serve as a primary point of contact between Krieger Scientific, client management, Calibration Technicians, and outside calibration providers.
- Maintain visibility into calibration status, upcoming requirements, overdue activities, resource needs, and potential program risks.
- Support the management of a large instrument and equipment population across multiple client locations.
- Oversee calibration records and related documentation to support compliance with Good Documentation Practices, ISO standards, GMP requirements, and other applicable regulatory requirements.
- Support the identification, documentation, escalation, and resolution of out-of-tolerance conditions, deviations, and other calibration-related issues.
- Work with the client and Calibration Technicians to determine which calibration activities can be performed internally and which require specialized outside services.
- Coordinate and manage outside calibration vendors when external services are required.
- Identify opportunities to increase internal calibration capabilities when practical while maintaining appropriate quality and compliance standards.
- Support the effective use and ongoing management of Blue Mountain or other computerized maintenance and calibration management systems used by the client.
- Help maintain accurate equipment records, calibration schedules, work orders, calibration histories, and related information within applicable systems.
- Review calibration activities and documentation for completeness, accuracy, and compliance with established procedures.
- Monitor workload and priorities across the calibration team and adjust daily activities based on client needs and calibration requirements.
- Identify potential scheduling, staffing, equipment, vendor, or compliance issues and communicate them proactively to Krieger Scientific and client management.
- Identify and lead Continuous Improvement efforts for Krieger Scientific and the client.
- Support the development and improvement of calibration procedures, processes, workflows, and program documentation.
- Promote a strong culture of safety, quality, accountability, technical excellence, and regulatory compliance.
- Provide hands-on calibration support when appropriate based on workload, technical requirements, and client needs.
What We Are Looking For
- Experience developing and overseeing complex projects, implementing program workflows, and determining CAPA actions.
- Strong hands-on calibration or instrumentation experience within a GMP-regulated life sciences environment, including pharmaceutical, biotechnology, or medical device.
- Experience leading or coordinating calibration programs, projects, technicians, or technical service activities.
- Strong understanding of calibration practices, standards, traceability requirements, and Good Documentation Practices.
- Working knowledge of GMP requirements and the relationship between calibration, equipment performance, data integrity, and regulatory compliance.
- Experience with temperature, pressure, flow, weight, and other critical measurement parameters.
- Experience coordinating calibration schedules, work orders, priorities, and technical resources.
- Experience working with outside calibration vendors and determining when specialized external services are required.
- Ability to identify, document, communicate, and appropriately escalate out-of-tolerance conditions and other calibration-related issues.
- Experience with computerized maintenance or calibration management systems. Experience with Blue Mountain is helpful.
- Strong organizational skills with the ability to manage multiple priorities across a large instrument population and multiple locations.
- Strong problem-solving skills and the ability to identify practical opportunities for Continuous Improvement.
- Strong documentation skills and a disciplined approach to data integrity and regulatory compliance.
- Ability to provide clear direction and support to Calibration Technicians while maintaining a collaborative team environment.
- Strong client communication skills and the ability to work effectively with technical personnel, operations, quality, management, and outside service providers.
- Ability to work independently, make sound day-to-day decisions, and appropriately escalate issues requiring client or Krieger Scientific management involvement.
- Ability and willingness to work across multiple nearby client locations as required.
Requirements
- Project Management discipline certification is a plus (PMP, CSM, Prince2).
- Valid driver’s license.
- Reliable transportation.
- Proof of motor vehicle insurance.
- Must meet applicable prescreening health and safety requirements.
- Must successfully complete required drug and alcohol screening.
- Ability to lift up to 75 pounds.
Compensation
Competitive hourly compensation, commensurate with experience.
Work Authorization
U.S. work authorization required. Visa sponsorship is not available for this position.
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
To Apply
Send your resume to careers@kriegerscientific.com.
Position: Calibration Technician
Location: Southeastern Pennsylvania (on-site, client locations)
Employment Type: Full-Time, Hourly
Schedule:40 hours per week
About Krieger Scientific
Krieger Scientific is a full-service compliance and technical solutions firm serving life sciences organizations across the full asset lifecycle. With more than 35 years of industry experience behind its leadership and a proud commitment as a veteran-owned business, Krieger Scientific builds teams around programs and stays focused on what comes next for our clients and for the people who work with us.
About the Role
Krieger Scientific is hiring an experienced Calibration Technician to support active projects and service contracts with life sciences clients in the Exton, Pennsylvania area.
This is a full-time, hourly position scheduled for 40 hours per week and is part of a dedicated Krieger Scientific team supporting the client’s calibration program through a staff augmentation engagement.
This is a precision-focused role for a compliance-minded professional who understands the critical relationship between instrument accuracy, data integrity, and regulatory standing in a GMP environment.
The Calibration Technician will focus primarily on hands-on calibration activities while working closely with the Calibration Program Manager, other Krieger Scientific team members, and the client’s management team to support the ongoing calibration needs of the facilities.
What You Will Do
- Perform calibration of instruments and equipment within client facilities in accordance with established procedures, SOPs, manufacturer requirements, and applicable regulatory standards.
- Perform calibration activities across multiple equipment types and measurement parameters, including temperature, pressure, flow, weight, and other critical measurements.
- Maintain accurate calibration records and generate certificates of calibration in compliance with Good Documentation Practices, ISO standards, and other applicable regulatory requirements.
- Identify out-of-tolerance conditions, support deviation reporting and investigation activities, and communicate findings clearly to client and Krieger Scientific team members.
- Support the development and maintenance of calibration programs, procedures, equipment records, and schedules as needed.
- Identify and contribute to Continuous Improvement efforts for Krieger Scientific and its clients.
- Work closely with the Calibration Program Manager and client management team to execute established calibration schedules and priorities.
- Support the assessment of instruments and equipment to determine whether calibration activities can be performed internally or require specialized outside calibration services.
- Coordinate with the Calibration Program Manager when outside vendors or specialized calibration services are required.
- Accurately document completed work within the client’s maintenance and calibration management systems.
- Support calibration program activities within Blue Mountain or other maintenance management software used by the client.
- Support calibration activities across nearby client locations and travel between sites as required based on calibration schedules and business needs.
- Work collaboratively with client personnel, Krieger Scientific team members, and outside calibration providers as required.
- Maintain a strong focus on instrument accuracy, data integrity, safety, regulatory compliance, and business continuity.
What We Are Looking For
- Hands-on calibration experience in a GMP-regulated life sciences environment, including pharmaceutical, biotechnology, or medical device.
- Familiarity with common calibration standards and traceability requirements.
- Experience with temperature, pressure, flow, weight, and other critical measurement parameters.
- Strong documentation skills and a disciplined approach to data integrity and regulatory compliance.
- Ability to identify and properly document out-of-tolerance conditions.
- Ability to follow established procedures and work independently while functioning effectively as part of a larger calibration team.
- Ability to manage daily calibration priorities in an environment with a large instrument population and recurring calibration requirements.
- Familiarity with computerized maintenance or calibration management systems. Experience with Blue Mountain is helpful.
- Strong communication skills and the ability to work professionally with client personnel, Krieger Scientific team members, and outside service providers.
- Ability and willingness to work across multiple nearby client locations as required.
Requirements
- Valid driver’s license.
- Reliable transportation.
- Proof of motor vehicle insurance.
- Must meet applicable prescreening health and safety requirements.
- Must successfully complete required drug and alcohol screening.
- Ability to lift up to 75 pounds.
Work Schedule and Environment
- This is a full-time, hourly position scheduled for 40 hours per week.
- The position is primarily onsite at client facilities in the Exton, Pennsylvania area. Technicians should expect to work at different client locations based on scheduled calibration activities and business needs.
- The position is intended for a locally based technician and is not structured as an overnight travel assignment.
Compensation
Competitive hourly compensation, commensurate with experience.
Work Authorization
U.S. work authorization required. Visa sponsorship is not available for this position.
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
To Apply
Send your resume to careers@kriegerscientific.com.
1. Position Summary
The Director of Business Development and Operations is responsible for growing Krieger Scientific’s business and for the operational discipline that supports that growth. This is a senior, independent role working directly with the Founder and CEO to expand Krieger’s presence among life sciences organizations while ensuring every engagement is staffed, delivered, and managed with the accountability the Krieger name is built on.
This role sits at the intersection of business development, talent strategy, and operations. The person in this seat builds new client relationships and expands existing ones, and in partnership with the Head of People, helps define the organizational structure and proactive recruiting strategy Krieger needs to scale. At the same time, this role owns the operational KPIs, staffing, and delivery discipline that keep every engagement bespoke in approach and non-negotiable in accountability.
2. Core Responsibilities
2.1 Business Development
- Develop and execute Krieger Scientific’s business development strategy
- Identify, qualify, and secure new business opportunities among life sciences organizations
- Build and maintain relationships with current and prospective clients
- Expand existing accounts across Krieger Scientific’s service offerings
- Develop proposals, pricing, presentations, and contract terms
- Maintain accurate revenue forecasts and provide regular updates to the CEO
- Develop strategic partnerships that support Krieger Scientific’s growth
- Represent Krieger Scientific at client meetings, conferences, and industry events
2.2 Talent Strategy and Recruiting
- Partner with the Head of People to forecast hiring needs and align talent with client demand
- Identify current and future hiring needs based on the company’s strategic growth plans
- Work with the Head of People to develop and refine job descriptions that accurately define each role, its responsibilities, and the experience required for success
- Identify target companies, competitors, and key industry professionals who represent ideal recruiting targets for each position
- Participate in candidate interviews and hiring decisions to ensure each hire brings the technical expertise, leadership ability, and cultural fit needed to strengthen the organization
- Help build a proactive talent strategy by identifying future organizational needs before they become immediate hiring requirements
- Partner with the Head of People to continuously evaluate organizational structure, succession planning, and leadership needs as the company grows
2.3 Operational Performance
- Oversee operational performance across active projects and client engagements
- Establish, track, and report operational KPIs
- Monitor project staffing, utilization, timelines, profitability, and client satisfaction
- Identify operational issues and put processes in place to address them
- Build repeatable processes that support company growth
- Improve communication and coordination across business development, recruiting, and project delivery
- Provide the CEO with recommendations related to growth, operations, staffing, and client delivery
3. Operational KPIs
The Director of Business Development and Operations will be responsible for developing and managing KPIs that may include:
- Revenue growth
- New client acquisition
- Expansion of existing accounts
- Proposal activity and close rates
- Revenue forecasting accuracy
- Project profitability
- Employee and contractor utilization
- Project staffing and time to fill
- Project delivery against schedule and budget
- Client satisfaction and retention
- Operational efficiency
4. Qualifications
Required
- Experience in business development within life sciences organizations
- Experience managing operations within a consulting, engineering, technical services, or project-based organization
- Experience selling consulting or technical services
- Knowledge of the life sciences consulting market and its major service providers
- Existing relationships within life sciences organizations
- Understanding of CQV, engineering services, quality and compliance, calibration, asset management, relocation services, technical staffing, or related services
- Experience developing proposals, pricing services, negotiating contracts, and managing client relationships
- Experience establishing and managing operational KPIs
- Demonstrated ability to build, mentor, and develop high-performing teams
- Experience identifying organizational talent needs and partnering in the hiring process
- Ability to clearly define role requirements and identify the technical and leadership competencies required for success
- Strong understanding of the competitive life sciences talent market
- Strong communication, organization, and leadership skills
- Ability to work directly with the CEO and across all areas of a growing company
- Ability to travel as needed
5. Success in This Role
- Generate profitable revenue growth
- Develop new client relationships and expand business within existing accounts
- Improve forecasting and visibility into future revenue
- Establish and manage meaningful operational KPIs
- Improve project staffing, utilization, delivery, and profitability
- Build processes that support continued growth
- Strengthen coordination between business development, recruiting, and operations
- Maintain strong client relationships and a high level of client satisfaction
- Build a strong partnership with the Head of People to identify, attract, and hire exceptional talent that supports Krieger Scientific’s growth strategy
- Develop clear organizational structures and role definitions that enable the company to scale effectively
- Help build a leadership team capable of supporting Krieger Scientific’s long-term growth
- Develop a repeatable talent strategy that identifies where the industry’s best people work and creates a proactive recruiting plan around those organizations
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
Position: Validation Engineer
Location: New Jersey (on-site, client locations)
Type: Contract
About Krieger Scientific
Krieger Scientific is a full-service compliance and technical solutions firm serving life sciences organizations across the full asset lifecycle. Founded by a 35-year industry veteran and proudly veteran-owned, we build teams around programs and stay focused on what comes next — for our clients and for the people who work with us.
About the Role
We are seeking an experienced Validation Engineer to support active projects with life sciences clients in New Jersey. This is a hands-on role for a compliance-minded professional who understands regulated environments and brings both technical depth and documentation discipline to every engagement.
What You Will Do
- Work directly within client facilities to plan, execute, and document validation activities across equipment, processes, and utilities.
- Collaborate with client quality and operations teams to ensure compliance with applicable regulatory requirements and internal SOPs.
- Author and review validation protocols, reports, and supporting documentation in accordance with GMP and GDP standards.
- Identify and communicate compliance risks proactively and support deviation management as needed.
What We Are Looking For
- A background in validation within a regulated life sciences environment — pharmaceutical, biotechnology, or medical device.
- Experience with equipment qualification, process validation, cleaning validation, or related disciplines.
- Strong documentation skills and familiarity with FDA and applicable global regulatory standards.
- Ability to work independently within client environments while maintaining clear communication with the Krieger team.
Compensation
Competitive, commensurate with experience.
Work Authorization
U.S. work authorization required. Visa sponsorship is not available for this position.
To Apply
Send your resume to careers@kriegerscientific.com or reach out to Joe Morwald directly. Specific project requirements will be shared with qualified candidates.
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
Position: Validation Technician
Location: New Jersey (on-site, client locations)
Type: Contract
About Krieger Scientific
Krieger Scientific is a full-service compliance and technical solutions firm serving life sciences organizations across the full asset lifecycle. Founded by a 35-year industry veteran and proudly veteran-owned, we build teams around programs and stay focused on what comes next — for our clients and for the people who work with us.
About the Role
We are seeking a Validation Technician to support active projects with life sciences clients in New Jersey. This is a hands-on execution role for a detail-oriented professional who takes compliance seriously and understands the importance of accurate, thorough documentation in a regulated environment.
What You Will Do
- Execute validation protocols under the direction of project leadership, including installation, operational, and performance qualification activities.
- Record data accurately in accordance with Good Documentation Practices.
- Support protocol preparation, test execution, and final report compilation.
- Work within client SOPs and quality systems while maintaining Krieger’s standards for accountability and rigor.
What We Are Looking For
- Hands-on experience in a GMP-regulated life sciences environment.
- Familiarity with IQ, OQ, and PQ execution and documentation.
- Strong attention to detail and a disciplined approach to data integrity.
- Ability to work effectively within client facilities and communicate clearly with both client and Krieger team members.
Compensation
Competitive, commensurate with experience.
Work Authorization
U.S. work authorization required. Visa sponsorship is not available for this position.
To Apply
Send your resume to careers@kriegerscientific.com or reach out to Joe Morwald directly. Specific project requirements will be shared with qualified candidates.
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
Position: Calibration Technician
Location: New Jersey (on-site, client locations)
Type: Contract
About Krieger Scientific
Krieger Scientific is a full-service compliance and technical solutions firm serving life sciences organizations across the full asset lifecycle. Founded by a 35-year industry veteran and proudly veteran-owned, we build teams around programs and stay focused on what comes next — for our clients and for the people who work with us.
About the Role
We are seeking an experienced Calibration Technician to support active projects with life sciences clients in New Jersey. This is a precision-focused role for a compliance-minded professional who understands the critical relationship between instrument accuracy, data integrity, and regulatory standing in a GMP environment.
What You Will Do
- Perform calibration of instruments and equipment within client facilities in accordance with established procedures, SOPs, and applicable regulatory standards.
- Maintain accurate calibration records and generate certificates of calibration in compliance with Good Documentation Practices.
- Identify out-of-tolerance conditions, support deviation reporting, and communicate findings clearly to client and Krieger team members.
- Support the development and maintenance of calibration programs and schedules as needed.
What We Are Looking For
- Hands-on calibration experience in a GMP-regulated life sciences environment — pharmaceutical, biotechnology, or medical device.
- Familiarity with common calibration standards and traceability requirements.
- Experience with temperature, pressure, flow, weight, and other critical measurement parameters.
- Strong documentation skills and a disciplined approach to data integrity and regulatory compliance.
Compensation
Competitive, commensurate with experience.
Work Authorization
U.S. work authorization required. Visa sponsorship is not available for this position.
To Apply
Send your resume to careers@kriegerscientific.com or reach out to Joe Morwald directly. Specific project requirements will be shared with qualified candidates.
Equal Employment Opportunity
Krieger Scientific LLC is an Equal Opportunity Employer. Employment decisions are made without regard to any characteristic protected by applicable federal, state, or local law. We will provide reasonable accommodations as required by applicable law. This job description describes the position’s general responsibilities and requirements and does not create a contract or guarantee employment. Duties and requirements may change based on business, client, regulatory, or operational needs.
Don’t see the right fit yet?
If you have deep expertise in life sciences compliance, calibration, CQV, quality, or operations and believe your background aligns with where Krieger is headed, we are always interested in hearing from experienced professionals.
Send your resume and a brief note about your background to:
careers@kriegerscientific.com
