QC Regulatory & Stability Area Specialist
Merck
About the Department For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. Being part of Novo Nordisk allows our employees to embark on the opportunity to help improve the quality of life for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. SDF maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies. What we offer you: Leading pay and annual performance bonus for all positions All employees enjoy generous paid time off including 14 paid holidays Health Insurance, Dental Insurance, Vision Insurance - effective day one Guaranteed 8% 401K contribution plus individual company match option Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave Free access to Novo Nordisk-marketed pharmaceutical products Tuition Assistance Life & Disability Insurance Employee Referral Awards At Novo Nordisk, you will find opportunities, resources, and mentorship to help grow and build your career. Are you ready to realize your potential? Join Team Novo Nordisk and help us make what matters. The Position Responsible for supporting the stability & retain programs for Quality Control site. Support process & drive improvement activities based on process performance, event response & process confirmation. Ensures audit readiness & shares ideas & solutions with other departments & sites. Relationships Reports to Manager, Quality Control Support. Essential Functions Responsible for preparing & updating stability protocols & reports Trend stability data & initiate trend investigations Responsible for providing stability & retain reports to corporate for annual product reviews Track & ensure stability testing is completed on time Write stability documents to support regulatory submission for new products Write stability documents for all other regulatory requests Support LIMS builds & training Maintain stability & reference sample inventory (storage & discard of samples) Stability representative during audits/inspections Project team member for new product transfers Other duties as assigned Physical Requirements Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Ability to do close precision work with their hands. Must be able to remain in a stationary position (sitting and standing) 50% of the time. May required corrected vision to 20/25 based on role. May require color vision based on role. Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. Qualifications Bachelor's Degree in Chemistry or related scientific field preferred or equivalent education & experience required Minimum of two (2) years of experience with stability programs &/or regulatory relevant experience preferred Strong communication skills (verbal & written) & the ability to author scientific & technical reports preferred Must demonstrate attention to detail, proofreading & strong computer skills with a willingness to learn new IT applications preferred Ability to control all aspects of the stability & retain programs a plus We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk, we're not chasing quick fixes - we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger - a legacy of impact that reaches far beyond today. Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at View phone number on click.appcast.io. This contact is for accommodation requests only and cannot be used to inquire about the status of applications. #J-18808-Ljbffr Merck & Co.
- ...Referral Awards The Position Responsible for supporting the stability & retain programs for Quality Control site. Support process &... ...testing is completed on time Write stability documents to support regulatory submission for new products Write stability documents for all...RegulatoryLocal area
- ...Nordisk seeks a Quality Control Support professional in Durham, NC, to manage stability and retain programs. Responsibilities include preparing documentation and ensuring compliance with regulatory standards. The ideal candidate will have a Bachelor's Degree in Chemistry...Regulatory
- ...Durham, NC is looking for a dedicated professional to support stability and retain programs for Quality Control. Responsibilities include... ..., conducting data analysis, and ensuring compliance with regulatory standards. The ideal candidate has a Bachelor's Degree in Chemistry...Regulatory
$41.06 - $76.25 per hour
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$15 per hour
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$18 - $26.49 per hour
...Comparative Medicine Specialist Work Arrangement: On-Site Location: Durham, NC, US, 27710 Personnel Area: MEDICAL CENTER School of Medicine Established in 1930, Duke... ...critical facility data daily as required by regulatory agencies and Duke standards and processes....RegulatoryWork experience placementWeekend work$36 - $39.26 per hour
...DEI & Innovation Advocate Job Title: EHS Specialist/EHS Coordinator Duration: 6 Months Job... .... Submit all EHS reports as required by regulatory authorities or the client requirements.... ...organization and be visible in the operational areas to support a safe and compliant work...RegulatoryHourly payContract workTemporary workFor contractorsInternshipWork at officeLocal areaShift work- ...chain, site and global Quality, and CMC‑Regulatory teams. It will be based in West Point, PA... ...franchise. Provide Subject Method Expertise to QC analysts and supervisors, assess impact... ...drug substance and drug product stability and release testing. Experience with analytical...RegulatoryContract workTemporary workFor contractors
$63k - $86.9k
...Position Summary: The Senior QC Analyst (2nd Shift) will be... ...characterization, release, or stability samples. Additionally, when... ...Ensures state of safety and regulatory audit readiness at all times... ...Laboratory support - ensures areas are neat, clean, organized, and...RegulatoryFull timeImmediate startMonday to FridayAfternoon shift- ...Novo Nordisk in Durham, NC is seeking a professional to support manufacturing operations and ensure compliance with business and regulatory standards. Ideal candidates will have a Bachelor’s degree in engineering or a related field, and at least three years of manufacturing...Regulatory
- .... Candidates should possess a Bachelor's degree in a scientific field and have at least 5 years of related experience. Skills in regulatory knowledge, communication, and problem-solving are essential. Offered benefits include medical, dental, vision, and a company bonus...Regulatory
- ...inpatient and/or outpatient therapy patient care areas; ensure effective delivery of clinical... ...with clinical patient care standards, regulatory requirements, and established policies... ...improve operational efficiency. Coordinate QC/PI activities with appropriate staff....Regulatory
- ...applications aligned with your capability area. You partner closely with Product... ...delivery, technical health, and operational stability of your applications and products while... ...platform sustainability.* Translate business, regulatory, and operational requirements into...Regulatory
- ...Why Work for WM? Stability. Growth. People-First Culture. About the Recycling Project Specialist Role Coordinates all onsite activities at client location in relation... ...to the education requirement). RCRA and DOT regulatory compliance experience strongly preferred. 24...RegulatoryContract workTemporary workWork experience placementWork at officeLocal area
$86.71k - $140.13k
...Location: Durham, NC, US, 27710 Personnel Area: MEDICAL CENTER School of Medicine... ...multiple affiliations. Be You. The Office of Regulatory Affairs & Quality (ORAQ) is seeking a GMP... ...serving as final signature authority for QC release of test results, raw materials,...RegulatoryWork experience placementWork at office$84.4k - $211.1k
...quality control processes Conduct quality control (QC) review of a wide range of Medical Writing... ...abreast of current data, trends, medical writing (MW)/regulatory knowledge, developments and advances in area of drug development/MW Qualifications: Bachelor...RegulatoryFull timeContract workPart timeWork at officeImmediate startWorldwide- ...associated with the Office of Regulatory Affairs and Quality in support... ...analytical in-process, release, and stability data and critical review of... ...reviews of GMP Analytical and QC Data review (75%) o... ...demonstrated successes in these areas. High level of accuracy in reviewing...RegulatoryFor contractorsWork at officeLocal area
- ...Job Description Why Work for WM? Stability. Growth. People-First Culture. About the Recycling Project Specialist Role Coordinates all onsite activities at... ...the education requirement). ~ RCRA and DOT regulatory compliance experience strongly preferred ~...RegulatoryContract workTemporary workWork experience placementWork at officeLocal area
- ...of relevant experience. You will coordinate various departments for efficient processing of change requests, ensuring quality and regulatory adherence. Benefits include a 401(K) match, medical and dental coverage, along with opportunities for professional growth. #J-18...Regulatory
$110k - $135k
...growth, which is why we have such stability in the group! Responsibilities... ...; coordinate and perform the QC of study reports and other... ...plans and reviews functional area plans Identify, evaluate, and... ...including but not limited to: regulatory binder review, source document...RegulatoryHourly payContract workRemote work
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