Manufacturing Superintendent

CA03 BioVectra Inc.; Charlottetown; On-site; CAD 94,000 - 146,000; Full time

Job summary

BIOVECTRA in Charlottetown, PEI, is hiring a Manufacturing Superintendent for nights (7 pm–7 am). Lead GMP production, oversee batch records, mentor staff, and drive on-time delivery while ensuring safety and quality in a multi-product operation.

The role involves after-hours availability, regulatory interactions, and collaboration across disciplines to optimize processes and schedules. A strong technical background and leadership experience are essential.

Qualifications

• High School Diploma.
• One year demonstrated technical experience.
• Ability to function and communicate in a dynamic, project driven team environment.
• Experience with various software programs, spreadsheets, and word processing.
• Demonstrated mature judgement and integrity of sensitive and confidential information.
• High degree of self-motivation, independence, maturity, and decision making.

Responsibilities

• Overseeing team leads in accomplishing overall departmental production needs and reviewing work to ensure consistency.
• 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.
• Supporting manufacturing schedules through appropriate documentation and staging requests.
• 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.
• Flexibility for after-hours consultation during manufacturing activities or during infrequent production activities will be required.
• Participating in client meetings and teleconferences.
• Providing guidance and oversight to a team of employees.

Skills

Team leadership

GMP experience

Regulatory understanding

Technical knowledge

Communication skills

Microsoft Office

Education

High School Diploma

Post-secondary degree or diploma in science

Tools

Microsoft Office

Excel

Job description

Job Description THIS IS A NIGHTS ONLY POSITION 7 pm-7am

BIOVECTRA, now a part of Agilent, is recognized as a leader in the contract development and manufacturing space of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI, plasmid DNA, mRNA, LNP and sterile filling capabilities. With over 650 employees at both the Windsor, NS and Charlottetown, PEI sites, BIOVECTRA supports over 100 clients, including over 20 top pharma and biotech companies. The Manufacturing Superintendent will supervise and lead a pharmaceutical manufacturing team in the various day to day functions and activities of GMP production, purification, isolation and packaging of synthetic chemical, natural extraction, and/or fermentation related products in a dynamic multi-product-based operation following all outlined safety practices, company protocols and objectives.

The responsibilities will include: Overseeing team leads in accomplishing overall departmental production needs and reviewing work to ensure consistency 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 Supporting manufacturing schedules through appropriate documentation and staging requestsEnsuring 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 Flexibility for after-hours consultation during manufacturing activities or during infrequent production activities will be required Participating in client meetings and teleconferences Providing guidance and oversight to a team of employees

Qualifications Required:

High School Diploma One year demonstrated technical experience Ability to function and communicate in a dynamic, project driven team environment Experience with various software programs, spreadsheets, and word processing Demonstrated mature judgement and integrity of sensitive and confidential information High degree of self-motivation, independence, maturity, and decision making

Desired:

Post-Secondary Degree or Diploma in a scientific field Two years demonstrated leadership experience Two years GMP experience, protocols and FDA guidance Five years of related technical experience

Additional Details

This job has a full time weekly schedule. The full-time equivalent pay range for this position is $93,521.00 - $146,126.00/yr CAD plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

• Ability to work 12-hour rotating shifts.
• Heavy lifting required (50 lbs.).
• Ability and willingness to work after hours and weekends if required.
• Required to use a respirator.

Travel Required: No Shift: Swing Duration: No End Date Job Function: Manufacturing Graduate and Student Career Site Visit our career site and learn more about Agilent! As a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. Leveraging more than 50 years of expertise, we create advanced instruments, software, and consumables supported by teams of highly skilled and knowledgeable people. With 18,000 employees around the world, our global reach and comprehensive solutions provide the most reliable and accurate results, as well as optimal scientific, economic, and operational outcomes. We work collaboratively with our customers on their journey to make a real difference in human lives. Our culture is founded on trust, respect, and uncompromising integrity, and we pride ourselves on being a dynamic and inclusive workplace that celebrates diversity and fosters innovation. We can't wait for you to join us as we continue our mission to improve the world around us. Information about Agilent is available at Agilent.com.