Manufacturing Team Lead

Accepting BioReady™: Yes
Category: Clinical Research
Education: Diploma/DEC
Location: Windsor, NS
Posted: June 30, 2020
Closes: July 30, 2020

Job description:

BioVectra Inc. has an opening for a Manufacturing Team Lead. This is a permanent, full-time position located in Windsor Nova Scotia.

The candidate will be responsible for:

  • Overseeing shift supervisors in accomplishing overall departmental production needs and reviewing work to ensure consistency with written standards.
  • Mentoring members of the production group and providing constructive input.
  • Reviewing the completed production records (ensuring all quality related documentation is signed and verified, QA review items are resolved and label requests have been completed).
  • Assisting in updates on batch production records (BPRs) to optimize process efficiencies and to assist in developing new BPR’s or work instructions.
  • Ensuring raw material and consumable counts are completed upon request.
  • Ensuring the equipment and processing areas are in an audit ready state to meet the posted schedule in compliance.
  • Identifying, troubleshooting and resolving equipment, process and facility issues as well as contributing to process risk assessments.
  • Participating in the hiring, training and performance evaluation of employees.
  • Participating in regulatory inspections and audits.
  • Interacting with multi-discipline units and personnel to ensure product quality and on-time delivery is adhered to.
  • Performing all manufacturing operation functions when required.
  • Managing the time and attendance software program and ensuring accuracy in all job costing activities.
  • Flexibility for after hour consultation during manufacturing activities or during infrequent production activities will be required.
  • Participating in client meetings and teleconferences.

The successful candidate for this position should have:

  • Grade 12 Diploma.
  • Post-Secondary Degree or Diploma (chemistry, biochemistry, biology, engineering) an asset.
  • Five years of related technical experience, chemical, pharma, or biotech processing is an asset.
  • Two years of demonstrated supervisory experience.
  • Knowledge of GMP, protocols and FDA guidance.
  • Experience with various software programs, spreadsheets, and word processing.
  • Closing Date July 7th 2020
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