TITLE: Lead CQV Specialist
REQUIREMENTS: Bachelor of Science or Master of Science in Industrial or Mechanical Engineering, Biotechnology, or related with 2 – 1 year experience as CQV Specialist respectfully. 2 years of experience working with MS Office suite (word, excel, powerpoint), quality tracking and document management (e.g. Veeva, Trackwise, SAP or KNEAT), and CFR 21 regulations and GMP and GDP.
JOB DUTIES: Develop and manage validation strategies, project plans, budgets and timelines, and supervise a team including task delegation, training, and employee growth. Draft, review, approve, execute protocols, and create operating procedures.
CONTACT: Send resume to:
MCA Services,
3908 Bishop Road,
Battleboro, NC 27809
Jobsite: Battleboro, NC (Full-Time Position)
