83 job opportunities for batch record in United States updated today
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· Page 2 / 5Piper Companies is currently seeking a QA Batch Record Reviewer for our Audubon, PA location. The QA Batch Record Reviewer is primarily responsible for batch record review and ensuring that operations are conducted in accordance with current Good Manufacturing Practice. Responsibilities include but
ProQuality NetworkPosition Summary We are seeking a detail-oriented and experienced Batch Record Reviewer to support a six-month on-site project. The selected candidate will be responsible for reviewing manufacturing batch records to ensure compliance with cGMP requirements, internal procedures, and regulatory standa
B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The co
Job DetailsJob Location: Scotts Valley Headquarters - Scotts Valley, CA 95066Position Type: Full TimeEducation Level: High SchoolSalary Range: $17.50 - $20.00 HourlyTravel Percentage: NoneJob Shift: DayJob Category: Supply ChainSummary of Job Duties: Under limited supervision, work closely with the
Nationwide Children's HospitalOverview: Job Description Summary: Job Description Summary Provide leadership in formulating regulation policy including resource management and development, implementation, and maintenance of a Quality Management Program for the Phase 1/2A IND, Biologics and Good Tissue Practice programs. Lead qual
Job Description Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! We are seeking Growth and Improvement minded SPO Technicians | Level 1 that can help drive our Strategic Operating Priorities. Invent | Pursue
Kelly Science, Engineering, Technology & TelecomKelly® Science & Clinical is seeking a Quality Assurance Associate for a 8-month contract opportunity with a leading biopharmaceutical company in South San Francisco, CA. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poise
*Location:** Onsite *Job Type:** Contract *Shift:** 1st or 2nd shift (must be flexible, including weekends and overtime as needed) *Pay:** $27 - $29 *Job Overview** We are seeking a Quality Assurance Associate to support batch record review and compliance activities within a biotechnology manufactur
Job Title: QS Associate I & II – Batch Record Auditor Location: Mainland, PA 19451 Hours: Monday-Friday, 8:00AM-5:00PM Join Our Team At Accupac, we are Makers. From formulation to manufacturing, we serve the most trusted brands in the beauty and personal care industries with a wide range of cosmetic
Amneal Pharmaceuticals*Description:** Review batch records for timeliness and accuracy. *Schedule:** *1st Shift 7am - 3:30pm Monday to Friday** *Essential Functions:** Perform final review of manufacturing documentation and provide support in areas of compliance for batch releases. Provide lot status updates as requested
Amneal PharmaceuticalsJob Description Description: Review batch records for timeliness and accuracy. Schedule: 1st Shift 7am - 3:30pm Monday to Friday Essential Functions: Perform final review of manufacturing documentation and provide support in areas of compliance for batch releases. Provide lot status updates as reque
Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughes
Fremont, CA Contract Duration: 6-24 months Rate: Negotiable Salary: NA $1.00 Responsibilities: Excellent employment opportunity for a Batch Record Writer in the Fremont, CA area. Creates manufacturing Batch record templates for multi-product. Writes, and edits technical documents related to bio-manu
Unternehmensbeschreibung Du willst Großes bewegen? Wir auch. Gemeinsam mit Dir. Gemeinsam Großes bewegen. Willkommen bei AbbVie! Als Teil eines internationalen Unternehmens mit 50.000 Mitarbeitern weltweit und rund 3.000 Mitarbeitern in Deutschland hast du die Möglichkeit, in enger Zusammenarbeit mi
General Information Name Quality Assurance Associate, Batch Record Review Employment Type Temporary Position level Part-time Virtual/Remote? No Labor Category Scientific Date 02-Apr-2026 City South San Francisco State California Country United States Ref # 9247853992 Description & Requirements Descr
Position Summary: Ensures the efficient and quality standards for operation of tablet press machinery and / or the capsule filling machinery. Maintains an orderly and clean facility in compliance with regulations and completes all paperwork associated with these tasks. Position Responsibility: Follo
Novo NordiskBatch Record Optimization Internship Facility: Education Location: West Lebanon, NH, US About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and grow
Vivex BiologicsJob Purpose The Quality Assurance (QA) Batch Record Reviewer performs the Technical and Final release function of the graft release process. The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a complia
About the Department Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life‑saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting‑edge medications. At
Job Purpose The Quality Assurance (QA) Batch Record Reviewer performs the Technical and Final release function of the graft release process. The QA Batch Record Reviewer performs functions necessary to assure that all relevant manufacturing records are assembled, reviewed, and completed in a complia
$40,000 – $63,000per year
Estimation confidence: Low
Estimate based on market data. Actual salaries may vary depending on experience, company, and location.