Principal - QA API External Manufacturing Peptides
$65.25k - $169.4kEli Lilly
Job Summary This role provides essential Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for all products manufactured by third-party partners. Job Responsibilities Lead and manage quality aspects of external API manufacturing sites, including but not limited to batch record review, disposition, deviation management, and change control. Conduct and/or participate in quality audits of external manufacturing sites to assess compliance with cGMP, regulatory expectations, and Eli Lilly's quality standards. Review and approve quality-related documents, such as manufacturing master batch records, validation protocols and reports, stability data, and analytical methods. Collaborate cross-functionally with internal teams (e.g., Supply Chain, Regulatory Affairs, Technical Services) and external manufacturing partners to resolve quality issues and drive continuous improvement. Provide expert QA guidance and support during new product introductions and technology transfers to external manufacturers. Develop, implement, and maintain quality agreements with external manufacturing organizations. Investigate and troubleshoot complex quality incidents, deviations, and out-of-specification results, determining root causes and implementing effective corrective and preventive actions (CAPAs). Represent Eli Lilly's quality interests during regulatory inspections at external manufacturing sites. Mentor and provide technical guidance to junior QA associates. Basic Requirements Bachelor's degree in Chemistry, Biochemistry, Pharmacy, Chemical Engineering or related scientific discipline. Minimum 5 years experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, with a strong focus on API manufacturing and external supply. Experience in cGMP regulations (FDA, EMA, HPRA, etc.) and global pharmacopeial requirements. Experience in auditing external manufacturing sites. Experience in quality management systems (e.g., Veeva). Willingness to travel domestically and internationally to external manufacturing sites as required. Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1. Additional Preferences Strong understanding of API manufacturing processes, analytical techniques, and quality control principles. Demonstrated ability to make sound quality decisions and effectively communicate complex technical and quality information to diverse audiences. Excellent problem-solving, analytical, and critical thinking skills. Ability to work independently and as part of a team in a fast-paced, dynamic environment. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #J-18808-Ljbffr Eli Lilly
$65.25k - $169.4k
...A global pharmaceutical leader seeks a Quality Assurance professional to oversee API external manufacturing operations. This role involves ensuring compliance with cGMP and regulatory requirements throughout the manufacturing process. The ideal candidate will have a strong...Suggested- Bavarian Nordic is seeking a Senior QA Specialist, External Manufacturing, to join their remote team. This pivotal role ensures compliance and product quality across sterile fill-finish operations and fosters a robust quality culture within the organization. The ideal candidate...SuggestedRemote job
- ...professionals ensuring compliance and quality oversight across external manufacturing of p roducts and devices. In this role you will be subject... ...People Leadership, Process Improvements, Quality Assurance (QA), Quality Management Systems (QMS), Regulatory Compliance,...SuggestedFull timeFor contractorsWork at officeLocal areaRemote workRelocationVisa sponsorshipFlexible hoursShift work
$55k - $86.9k
...JOB SUMMARY The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas... ...reconciliation Alarm response and acknowledgement Support external client review and resolution of comments JOB...SuggestedContract workImmediate startShift work- ...SME for the Quality team reporting cross-QA metrics and status for KBI and clients. The... ...with all functions supporting the external network, including interaction with functions... ..., policies, and guidelines governing the manufacture and holding of materials for our company....PrincipalImmediate startFlexible hours
$113k - $156k
## KBI: US - Principal QA SpecialistApplylocations: USA - NC - Durham - Hamlin Rdtime type:... ...exemplary service to both internal and external customers by ensuring patient safety and... ...with clients, laboratories, manufacturing, QA batch disposition and other internal...PrincipalImmediate start- ...Deviations and CAPAs in support of GMP manufacturing operations and other functional groups as... ...initiation in EtQ and closure. Mentors junior QA staff in deviation/CAPA review and... ...Notifies the Client of deviations. Supports external client review and resolution of comments...Principal
- Principal Quality Compliance Specialist Deviations and Client SupportSkip... ...and CAPAs in support of GMP manufacturing operations and other... ...and closure. Mentors junior QA staff in deviation/CAPA review... ...Client of deviations. Supports external client review and resolution...PrincipalImmediate start
- ...automation frameworks and ensure system quality in a collaborative environment. The ideal candidate has over 5 years of experience in API testing and Java development, along with strong knowledge of AWS Cloud services and SQL. This role offers the opportunity to improve...
$126k - $234k
...Summary Drive the future of gene therapy manufacturing and make a meaningful impact on patients' lives. As a Principal Engineer, MS&T, you will serve as a... ...manufacturing issues across internal operations and external partners (CMOs) Mentor and develop MS&T staff...PrincipalRelocation package- Staff Engineer - QA Automation [ 14 - 17 years exp] Nutanix has disrupted the multi-billion-dollar virtualization market by pioneering... ...white-papers and blogs, file patents, represent Nutanix in external seminars. What You Will Bring Familiarity with OS internals, concepts...Work experience placementWork at officeRemote work3 days per week
- ...and skills gaps, our staffing experts can help you find the best job for you. Role: QA Automation Engineer Location: Remote Duration: 6 month Required Skills:API Job Description: Role will work closely with developers, product owners, SMEs, and...Permanent employmentContract workRemote work
$126k - $234k
Drive the future of gene therapy manufacturing and make a meaningful impact on patients’ lives. As a Principal Engineer, MS&T, you will serve as a scientific and technical... ...issues across internal operations and external partners (CMOs). Mentor and develop MS&T staff...PrincipalRelocation package- ...A renewable energy solutions provider based in North Carolina is seeking a Principal Software Engineer. The role involves designing, developing, and deploying software for Battery Energy Storage Systems (BESS). Candidates should have 6+ years of software engineering experience...PrincipalRemote work
- ...Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity... ...Materials Planning, Warehouse, and QA/QC, teams while helping to resolve any problems... ...leadership with both internal and external customers/suppliers. Proven oral and...Flexible hours
- ...regulations. Responsibilities include conducting investigations, providing training, and driving process improvements in a pharmaceutical manufacturing environment. Ideal candidates will have a Bachelor’s degree in engineering or related fields, along with GMP knowledge and at...
$50 - $65 per hour
...Test to design, develop, and maintain automated test suites for digital healthcare products. The role requires strong skills in UI and API automation using Playwright or Cypress, along with TypeScript or JavaScript. Candidates will engage in Agile practices and...Hourly payFlexible hours- ...Analyst. This role involves ensuring the accuracy and quality of insurance products through comprehensive testing, particularly with APIs. The ideal candidate has a solid background in the Life/Annuity domain and will collaborate with teams to meet both functional and...Full time3 days per week
- ...MACOM designs and manufactures semiconductor products for Data Center, Telecommunication,... ...entire portfolio. Reliability Engineer- Principal Job Description The Principal Reliability... ...and non-technical internal and external customers Qualifications Bachelor’s Degree...PrincipalPermanent employmentTemporary work
- ...Our client, a leading Medical Device Manufacturing Company is looking for Quality Control - Inspector 2 and This is for an initial... ...capabilities. Effectively communicate with internal and external customers. Interact within a team environment. Perform...Hourly payContract work
- ...the review and approval of Deviations and CAPAs to support GMP manufacturing operations. This position involves collaborating with various departments... ...resolve compliance issues and providing mentorship to junior QA staff. The ideal candidate will possess a scientific degree and...
- ...A leading pharmaceutical company is seeking a quality assurance professional to oversee compliance in manufacturing and product release. This role requires a Bachelor’s Degree in Life Sciences and a minimum of 5 years experience in the pharmaceutical industry focusing...
- ...QA Manufacturing Specialist Please Note: This is a day shift opportunity that follows a 2-2-3 schedule The QA Manufacturing Specialist is responsible for ensuring raw materials, products, processes, facilities, documentation, and systems conform to quality standards...Work at officeImmediate startDay shift
- ...QA Validation Specialist Location: Research Triangle Park, NC – 27709 Duration: 10 Months Pay Rate: $45/hr - $53/hr on W2 The... ...in pharmaceutical, biotech, or biologics GMP regulated manufacturing environment with 3+ years in Quality and/or Manufacturing. ~...For contractorsWork at officeFlexible hours
$113k - $156k
...approval of in-process, release, and stability test data. The Principal QA Specialist provides QA oversight of analytical and microbial... .... The specialist collaborates with clients, laboratories, manufacturing, QA batch disposition, and other internal stakeholders to achieve...Principal- ...firm located in North Carolina is looking for an experienced Quality Assurance professional. The role involves providing QA support to manufacturing processes, reviewing, and approving critical documentation. Candidates should have a Bachelor's degree and over 8 years of...
$20 - $22.88 per hour
...Corning Inc. seeks a Manufacturing Associate for the 12hr Day Shift in Durham, NC. This position requires a High School Diploma or GED and 6-12 months experience in a manufacturing environment. Responsibilities include operating production equipment, maintaining safety...Hourly payDay shift- ...Assurance provides essential day-to-day QA support to the analytical laboratories. This... ...is a global provider of chemistry, manufacturing, and control (CMC) analytics to the life... ...material testing to drug product release and API development for small molecules. Headquartered...Full timeContract workRelocation
- Novartis Farmacéutica is seeking a Principal Engineer, MS&T in Durham, NC, to lead technical efforts in gene therapy manufacturing. The role involves guiding cross-functional collaborations and ensuring high-quality production of innovative therapies. Ideal candidates will...Principal
- ...experienced Insurance Quality Analyst. The ideal candidate will have 6+ years in the Life/Annuity domain and a strong understanding of API testing. Responsibilities include ensuring the quality of insurance products, testing both front-end functionalities and backend APIs...3 days per week
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