Actalent ยท 2 days ago
Document Control Specialist
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Business DevelopmentBusiness Information Systems
Insider Connection @Actalent
Responsibilities
Pre-production preparation, review, and approval of batch records for various cGMP OTC, medical device, and pharmaceutical products
Post-production batch record review and approval
Review production data and draft COA and COC from this data using approved templates
Trend data collected from batch records and update periodically
Diagnose and propose areas of growth within current QMS
Print, scan, file, and archive batch records and other quality documents
Support the Director of Quality with quality-related activities
Work smoothly within a devoted team
Qualification
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Required
Bachelor's degree in science related field (MS preferred)
2+ years in like or similar function in pharmaceutical or medical device industry cgmp
Strong communications skills and proficiency with the English language, specifically scientific, pharmaceutical, and medical device nomenclature
Experience working in a cGMP environment
Experience working with and familiarity with cGMP quality documentation such as batch records, NCRs, CAPAs, SOPs, DCRs, COAs, COCs, etc.
Company
Actalent
Actalent is an engineering and sciences service company.
H1B Sponsorship
Actalent has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Trends of Total Sponsorships
2023 (31)
2022 (63)
2021 (20)
Funding
Current Stage
Late StageLeadership Team
Recent News
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