Log In
Sign Up
Jubilant HollisterStier LLC, a well-established member of the business community in Spokane, Washington, provides a complete range of services to support the pharmaceutical and biopharmaceutical industries. The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma. Jubilant HollisterStier is also a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products. Jubilant HollisterStier is a proud member of the Jubilant Pharma family.
Our Promise: Caring, Sharing, Growing
We will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions’ through growth, cost effectiveness and wise investment of resources.
Job Description:
The Stability Supervisor I position provides direction and support of the daily operations in the Stability Group of Quality Control through scheduling, assignment of tasks among the associates, and review and approval of the stability s, associated documents, and records. The individual in this position will maintain a program to ensure the appropriate training, and associated documentation, of Stability Associates (including safety, cGMP, and job functions). Input and support for Stability related investigations, and completion of necessary documentation, is also expected. Essential responsibilities include:
- Coordinate and schedule the Stability testing performed in the Analytical/Microbiological Quality Control Laboratory. This includes routine testing associated with approved products and testing performed for developmental or trial manufactured products.
- Provide Annual Stability Demand to Planning Department and manage the ordering and receipt of required batches. This requires close cooperation with Production Inventory Control and Manufacturing Departments.
- Oversee the training of Stability Associates, which includes maintaining the training program, conducting the training, documenting the training, and ensuring that the training program is in compliance with applicable procedures. The training encompasses safety, cGMPs, job functions, and new and revised standard operating procedures.
- Review and approve the stability study set up in the stability management software. Review and approve stability s prior to issuance from the laboratory; this includes review and approval of data trends, study summaries, and associated documentation.
- Provide input and oversight on Stability Plans and Protocols for new projects and ensure compliance with established plans for existing products.
- Supervise and assist the associates as they solve technical problems.
- Complete the Performance Reviews for each direct- including objective setting.
- Conduct periodic audits of procedures used within the laboratory to ensure that associates are performing in accordance with the procedures and that said procedures are written accurately and reflect the actual processes involved.
- Assess and recommend processes to improve efficiencies and compliance in the laboratory and Stability Department.
- Serve as a Quality Unit Representative on project teams as needed to support Contract Manufacturing/Allergy Business Unit.
Qualifications:
- Bachelors of Science in Biology, Chemistry, Microbiology, or related field. In lieu of degree, 3 years of Stability Experience and 2+ years of Pharmaceutical Experience is required
- Minimum 3 years related experience required.
- Demonstrated professional or academic project management experience or lead/leadership experience desired. Supervisory experience desired.
- Pharmaceutical and laboratory experience desired.
- Experience with Stability Programs, Stability Protocols, and ICH requirements strongly desired.
- Experience with Microsoft Word, Excel, and PowerPoint required.
- Experience with cGMP concepts, as related to laboratory and facility operations required.
- Must be able to work effectively with peers from other departments, on project teams, and with those individuals who directly to this position.
- Must be able to develop and effectively present training programs for the laboratory personnel that relate to safety, cGMPs, and job training.
- Physical Requirements: Prolonged sitting/standing, exposure to allergens and working in aseptic areas. Ability to lift 25 lbs. unassisted.
Shift: Day
Compensation:
- The salary range for this position is $72,026 – $106,002 depending on experience.
Benefits:
- Medical, Dental, Vision, Flexible Spending and Health Savings Accounts
- Life, AD&D, Short and Long Term Disability
- 401(k) with company match
- Generous paid time off plan
- Employee Assistance Program
Optional Benefits:
- Voluntary Life and AD&D for employee & family
- Supplemental Medical coverage (Critical Illness, Hospital Indemnity and Accident coverages)
- Pet Insurance
- ID Theft Protection
- Perk Spot Discount Program
Jubilant HollisterStier is a great place to grow!
If you’re up for a rewarding challenge, we invite you to take the first step and apply today!
https://www.jublhs.com/careers/career-opportunities
*Please click on the Spokane, WA link*
Jubilant HollisterStier is an EEO/AA Employer.
All qualified applicants will receive consideration for employment without regard to their protected veteran status and will not be discriminated against on the basis of disability.
If you require assistance applying for a position, please contact our HR Department at:
