Pharma Technical Writer - Quality & Investigations
Sun Pharmaceutical Industries Ltd
Sun Pharma in New Jersey seeks a Technical Writer to support investigations and QA records in manufacturing and packaging operations. You will assist cross-functional investigations for OOS, OOT, CAPAs, and change controls, ensuring timely closure and alignment with QA documentation standards. Requirements include a Life Sciences or Pharmacy degree, strong communication, project management skills, and familiarity with GDP/GMP. #J-18808-Ljbffr Sun Pharmaceutical Industries Ltd
$45 - $49.65 per hour
job summary: Join a top-tier global pharma leader in Branchburg, NJ, as a Supply Chain Technical Writer II. This 6-month extendable contract role offers an excellent... ...gaps and duplication. Collaborate with Quality and Supply Chain teams to ensure all documentation...QualityHourly payContract workTemporary workWork experience placementWork at office- ...SUMMARY/OBJECTIVE: The Technical Writer, Analytical is responsible for supporting and coordinating Quality Management System (QMS) documentation activities for the laboratory... ...with laboratory-related deviations, investigations, CAPA, and change control documentation....QualityFull timeWork at officeWork from home
$80k - $110k
...SUMMARY/OBJECTIVE: The Technical Writer is responsible for leading Quality Management System (QMS) documentation activities within Operations. This role... ...Root Cause Analysis and CAPA development for GMP investigations. Leads change control documentation activities...QualityFull timeWork at office- ...Technical Writers A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well... ...inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality...QualityImmediate start
- ...Technical Writer III A Few Words About Us Integrated Resources, Inc is a premier staffing... ...mission centers on delivering only the best quality talent, the first time and every time.... ...management system Help with investigations, non-conformances and CAPA process...QualityWork at office
$43 per hour
...is immediately hiring for a Regulatory- Technical writer. Position type: Full-time- Contract... ...authors/ authors scientific content for CTD Quality sections aligned with regulatory... ...final publication. Experience in biotech/pharma e2e product development required. Must...QualityHourly payFull timeContract workTemporary workWork experience placementWork at officeImmediate startWorldwideFlexible hours$38 - $41.96 per hour
The Technical Writer and Document Specialist (TW/DS) will sit within the Cell Therapy Development (CTD) Project and Portfolio Management Office... ..., Analytical Development, Cell Therapy Technical Ops, Quality and Regulatory Sciences across CTDO. The successful candidate...QualityHourly payContract workTemporary workWork at officeLocal area- Sun Pharma seeks a Technical Writer to support investigations and assist manufacturing and packaging operations on investigations, product quality complaints, and change controls. You will participate in cross-functional investigations, drive improvements in KPIs, and...Quality
$71.3k - $132.5k
...Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open... ...Position Join our dynamic cross-functional team as a Senior Technical Writer, where you will drive product launch success and operational...QualityLocal areaRelocation package- US Pharma Lab, Inc. is hiring for an Associate, In-Process Quality Assurance MFG/PKG in North Brunswick, NJ. The IPQA roles cover Level 1-3 responsibilities across manufacturing and packaging operations, with emphasis on GMP compliance, line clearance, and real-time documentation...QualityWeekend work
- Amneal Pharmaceuticals is hiring a Quality Assurance Inspector II for the 2nd Shift at their Piscataway Township location. This role involves monitoring and ensuring the quality of raw materials and drug manufacturing processes, maintaining records, conducting inspections...QualityHourly payAfternoon shift
- US Pharma Lab in North Brunswick, NJ is seeking a Chemist, QC I-III in a regulated FDA environment, performing analytical testing of... ...HPLC/UPLC, GC, ICP-MS, UV-Vis, FTIR, and dissolution, ensuring quality and timely release of materials. Extended hours may be required...Quality
- ...delivering only the best talent with integrity since 1996. We provide quality resources in Information Technology (IT), Clinical Research,... ...Therapy and Nursing. We place candidates in roles such as Technical Writers for Johnson & Johnson. Our mission centers on delivering...QualityImmediate start
- ...Job Title: Technical Writing Specialist Location: Warren, NJ, 07059 Duration:... ...grammar, punctuation, and overall document quality. Process oriented with solid... ...Experience writing protocol deviations, investigating out of specification results, performing...QualityContract workFor contractorsWork at officeImmediate start
- Sun Pharma is seeking a highly motivated Compliance Associate II to support and strengthen our Quality Management System (QMS) and site compliance programs. This role maintains regulatory compliance, drives quality system effectiveness, and supports inspection readiness...Quality
- US Pharma Lab, Inc. in North Brunswick, NJ, seeks an Associate Director of Quality Assurance Compliance to lead and strengthen QA programs, GMP/GLP compliance, and inspection readiness. You will shape SOPs, oversee audits, and mentor the QA team to support regulatory expectations...Quality
$235k - $255k
...Junction, NJDescriptionTris Pharma, Inc. ( is a leading privately... ...an experienced R&D/Clinical Quality leader to oversee our small QA... ...management, CRO activities. Investigator site/CRO audits/Vendor audits... ...industry in positions of increasing technical responsibility (minimum 8 of...QualityFull timeContract workWork at officeLocal area- ...Technical Writer We at Software Technology Inc. are hiring for a Technical Writer. If you are interested and a good fit, feel free to reach... ...Experience ~5+ years of Technical Writing for IT in Bio-Pharma ~5+ years Writing Business Requirement Documents ~3+...Local area
- ...Uspl Nutritionals Llc is seeking a Chemist, Quality Control in North Brunswick, NJ. The role focuses on routine chemical and physical... ..., maintain records, and support method validation and investigations. Entry-to-mid level experience is valued; standard hours plus...Quality
- ...productivity applications, with specific experience with Microsoft applications, and/or Zoom Meetings. Job will require ability to investigate and test functionality of the applications and turn that knowledge into usable guides for the J&J end User community. Writing...
- ...Road, North Brunswick NJ 08902 Title Associate, In-Process Quality Assurance MFG/PKG Department Quality Assurance Operation... .../rejected/quarantine). ???? Deviation & CAPA Management Investigate and document process deviations, non-conformances, and OOS/OOT...QualityImmediate startShift work
- ...Integrated Resources Inc. is seeking a Chemist to join their team in Edison, NJ. The ideal candidate will perform QC testing to assess the quality of pharmaceutical materials, ensuring compliance with regulatory standards. This entry-level position is ideal for science...Quality
- ...Description Job Description We are seeking an experienced Quality Assurance Lead to support daily food safety and quality... ...Plastic audits, and corrective-action follow-up. Assist with investigations, root-cause analysis, CAPA, customer complaints, product holds...QualityWork at officeFlexible hours
- ...popcorn. Job Summary We are seeking an experienced, hands-on Quality Manager to lead plant-level quality assurance, food safety,... ..., legality, or regulatory compliance may be compromised Investigation, Corrective Action & Continuous Improvement Lead investigations...QualityShift work
- ...Quality Technician IThe QA Technician at Cornerstone Building Brands is responsible for ensuring product quality, compliance with customer... ...Analysis (CFA), and Defect Material Report (DMR) processes.Investigate quality issues and participate in root cause analysis...Quality
$80k - $90k
...Position Title : Quality Assurance Manager Department: Quality Assurance Reports To: Director, Quality Assurance Position Summary... ...with implementation of e-QMS modules if required. Assist with investigations and deviations received from the manufacturing partners as well...QualityContract workTemporary workWork at officeLocal areaFlexible hours$118k - $158k
...longer destiny. Join Rocket Pharma. Rocket Pharma is a fully integrated... ...seeking aSenior Manager, Quality Control Operations to lead... ...cross-functionally with Technical Development, Regulatory, Manufacturing... .... Manage and support QC investigations, deviations, change controls...QualityContract workTemporary workLocal areaShift work$38 - $41.96 per hour
A leading biopharma company in New Jersey is seeking a Technical Writer and Document Specialist to support regulatory submissions for a late-stage clinical cell therapy program. Responsibilities include co-authoring scientific content, managing submission logistics, and...Hourly payContract work$100k - $145k
...Description Tris Pharma, Inc. ( is a leading privately-owned... ...has an immediate opening for Quality Engineer SUMMARY:... ...FDA 21 CFR 211.180(e) with technical engineering controls to ensure... ...conclusion Drives Root Cause Investigations by partnering with QA Investigations...QualityFull timeWork experience placementWork at officeImmediate startShift work- 50% onsite Job Function: The Quality Systems Manager is responsible for implementing... ..., metrics where applicable • Display technical knowledge of the process and understand... ...Processes include Deviation Investigations, Corrective Action / Preventive Action...QualityPermanent employmentContract workWork at officeLocal areaFlexible hours
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