Manufacturing Superintendent

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

Benefits offered by this job

Bonus

Stock options

Benefits package

Job summary

Agilent Technologies Inc. seeks a nights-focused manufacturing leader in Charlottetown, PEI. You will oversee production teams, mentor staff, and ensure BPRs, QA reviews, and regulatory compliance are met while maintaining production schedules.

Flexibility for after-hours and weekends is required. The role requires a high school diploma with 1+ year technical experience or a science-related post-secondary credential and leadership experience.

Qualifications

• High School Diploma required.
• Scientific post-secondary degree preferred.
• Demonstrated ability to work in a team and communicate effectively.
• Experience with spreadsheets and word processing.

Responsibilities

• Oversee production needs and review work for consistency.
• Mentor production staff and provide constructive input.
• Review and attach QA/BPR related documents; ensure approvals.
• Update batch production records and develop new work instructions.
• Support scheduling and material/solvent counts as needed.
• Ensure equipment and areas are ready to meet schedules.
• Identify and resolve equipment, process and facility issues.
• Participate in hiring, training, and performance reviews.
• Support regulatory inspections and audits.
• Interact with cross-functional teams to ensure quality and on-time delivery.
• Provide after-hours support as needed.
• Engage in client meetings and provide leadership guidance.

Skills

Leadership

Teamwork

Communication

Problem solving

Education

High School Diploma

Science degree (Post-Secondary)

Tools

MS Office

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.

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 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.

Required 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

Desired Qualifications

• 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