Manufacturing Team Lead
Ver: 235
Día de actualización: 12-06-2024
Ubicación: Charlottetown Prince Edward Island
Categoría: FMCG Artículos para el hogar Gerencia ejecutiva Producción / Operación Mantenimiento Mecánica / Técnica Farmacéutica / Química / Biotecnología
Industria: Pharmaceutical Biotechnology
Contenido de trabajo
- 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 BPRs (ensuring all QCs, deviations, cleaning sheets, etc. are attached to the BPR, BPR lines are 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 material and/or solvent counts are completed upon request.
- Ensuring the equipment and processing areas are in a ready state to meet the posted schedule.
- 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.
- Bachelor of Science degree or a College diploma in chemical, environmental, mechanical or industrial technology or equivalent work experience in the chemical/pharmaceutical processing industry.
- Five years of related technical experience.
- Two years of demonstrated supervisory experience.
- Knowledge of GMP, protocols and FDA guidance.
- Experience with various software programs, spreadsheets, and word processing.
Closing Date: October 22, 2021
Individual accommodations due to a disability are available upon request for candidates taking part in all aspects of the selection process. All qualified applicants will receive consideration for employment without regard to age, race, religion, ethnicity, gender, disability, citizenship status, marital status, actual or perceived sexual orientation.
BioVectra is committed to creating an inclusive environment and building a team that represents a variety of backgrounds, perspectives, and skills. We value diversity and recognize that experience comes in many forms and skills are transferable. Please view this description as a general overview, but not a mandatory comprehensive list. If you feel passionate about our efforts and believe that you have the skills to contribute and lead in this role, apply!
Plazo: 27-07-2024
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