1900 Technical Manager Quality Control jobs in Bloomfield,NJ

A minimum of a bachelor's degree is required. A focused degree in a science-related discipline is preferred.
A minimum of 8 years of experience working in a regulated industry is required.
Experience in over-the-counter drug and/or cosmetic manufacturing is highly desired. Experience with pharmaceutical and/or medical device manufacturing is a plus.
Working knowledge of cGMP requirements, current FDA enforcement issues and current regulatory authority enforcement practices is required.
Working knowledge of process validation, cleaning validation, manufacturing and packaging equipment train designs, microbiological controls, and assessing compliance to regulations is required.
Experience in managing quality activities for large volume external manufacturing and supplier sites ensuring compliance with applicable regulations.
Demonstrated ability to collaborate with internal and external partners to enhance relationships and interactions.
Experience in the facilitation of internal and external audits and regulatory inspections.
Demonstrated ability to build respectful and productive relationships with subordinates, peers, and leadership partners across multiple responsibility levels and within a high matrix structure is required.
Strong communication (verbal, written, and presentation) and interpersonal skills, self-awareness and adaptability required.
Demonstrated ability to lead as a key team member, developing strategy/plans and implementing successful outcomes is required.
Demonstrated ability to address complex issues using deductive reasoning, critical analysis skills and systematic approaches is required.
Demonstrated working knowledge of root cause analysis techniques including but not limited to: brainstorming, data collection and analysis tools, 5-whys, Fishbone (cause and effect), FMEA, and DMAIC is required.
Results-oriented with strong track record of success in delivering on objectives.
Ability to work in a fast-paced environment with multiple, concurrent priorities many needing immediate resolution.

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USA Documentation Specialist I Manufacturing Quality 1st Shift

Adecco

Pearl River, NY 10965

$35.46/hr

~ 37 min OnsiteHealth InsurancePaid Time OffRetirement Benefit

High School Diploma with 5+ years of relevant experience, OR
Associate Degree with 3+ years of experience, OR
Bachelor's Degree with 1+ year of relevant experience (including final-year candidates)
Experience in pharmaceutical, biotechnology, or regulated manufacturing environment required
Strong understanding of GMP, GDP, and documentation control principles
Experience with CAPA, deviations, and quality systems
Familiarity with technical documentation systems or ERP platforms
Strong attention to detail with ability to identify errors quickly and accurately
Excellent communication and interpersonal skills for cross-functional collaboration

SmartExplore AI is experimental.