Manufacturing Superintendent

Agilent Technologies; Charlottetown; On-site; CAD 94,000 - 146,000; Full time

Benefits offered by this job

Bonus eligibility

Stock options

Benefits

Job summary

Agilent Technologies at BIOVECTRA's Charlottetown site is seeking a Manufacturing Superintendent for a nights-only, 7 pm–7 am shift to supervise GMP production, purification, isolation and packaging across multiple products. The role leads a manufacturing team and ensures compliance with safety and quality standards.

Responsibilities include mentoring staff, maintaining batch records, supporting schedules and audits, and guiding process improvements while coordinating with cross-functional

Qualifications

• High School Diploma.
• One year demonstrated technical experience.
• Ability to function 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 to meet departmental production needs and ensure consistency.
• Mentoring members of the production group.
• Reviewing BPRs with QC, deviations, cleaning sheets, QA items.
• Updating batch production records to optimize processes and develop new BPRs or work instructions.
• Supporting manufacturing schedules through documentation and staging requests.
• Ensuring equipment and processing areas are ready to meet the posted schedule.
• Identifying and resolving equipment, process and facility issues; contributing to risk assessments.
• Participating in hiring, training, and performance evaluations.
• Participating in regulatory inspections and audits.
• Interacting with multi-discipline units to ensure product quality and on-time delivery.
• Flexibility for after-hours consultation during manufacturing activities.

Skills

Leadership

Team collaboration

Communication

Decision making

Self-motivation

Education

High School Diploma

Post-Secondary Degree in a scientific field

Tools

MS Office

Spreadsheets

Word processing

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

WORK CONDITIONS:

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.

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.

Travel Required:

No

Shift:

Swing

Duration:

No End Date

Job Function:

Manufacturing