Overview
You’re an energetic and collaborative force behind an innovative global manufacturing process – one that’s bringing high-quality medicines to the world. Together with your team, you’ll push for new approaches, test limits, and find the solution to every challenge. Join a workplace that values your contributions and stands behind your growth and success. When can you start?
Success Profile
What makes a great Compounder at Taro Pharmaceuticals? Take a look and see how you match up.
- Collaborative
- Industrious
- Logical
- Problem-solver
- Responsible
- Energetic
Our Culture
As a pioneering leader with an unwavering dedication to research and development, our environment is dynamic and collaborative. It’s also an ideal destination for your talents. We’ll nurture your creative spirit and help you unleash your potential. Join us and play a role while living our mission of shaping a healthier future for all.
Phani P. Senior Director, Production Operations“Pharmaceutical Manufacturing is the balance of providing accessible drug products and maintaining the highest quality standards. I’m proud to work in a place where my passion for producing the highest quality products is shared by everyone.”
Benefits
We’re in your corner – in so many different ways. Taro Pharmaceuticals wants you to have the benefits, support, and rewards of a job well done.
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Career Growth
Get support for your career growth and development.
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Benefits Programs
Discover comprehensive benefits to support the health and wellness of you and your family.
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Time Off
Enjoy paid time off and leave-of-absence options.
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Compensation
Earn competitive compensation with incentive programs that reward our shared success.
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Working Conditions
Work confidently in the safe, clean, and regulated work environment that we foster.
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Team Environment
Collaborate in a workplace that’s rooted in our values and encourages cross-team engagement.
Compounder
Brampton, OntarioGeneral Summary:
Responsible for the cleaning, setting up and operation of manufacturing equipment’s as part of the process of compounding pharmaceutical creams, ointments, gels and liquids.
Principal Duties and Responsibilities:
- Complete G.M.P. documents, such as the Batch Record, cleaning & sanitizing logs, housekeeping logs and other documents / log records pertaining to manufacturing
- Follow safety rules/regulations and report any workplace injuries or accidents. Assist when required to improve equipment safety related procedures. Wash and sanitize compounding rooms and vessels
- Compounding batches as per SOP’s and Master Formulas. Report discrepancies and deviations in a timely manner to compounding lead hand or supervisor
- Dispense raw materials when required
- Perform accurate inventory transactions using SAP
- Maintain a clean and organized working environment. Familiar with 5S processes and Lean Manufacturing Concepts
- Participate and assist with continuous improvement projects and processes
- Work safely and accurately with a focus on completing tasks and documentation right first time
- Complete all GMP Documentation correctly and in a timely manner
- Complete all training assignments and maintain personal training records
- Participate in and/or lead Non Conformance Investigations
- Complete Corrective and Preventive Actions (CAPA’s)
- Initiate, and follow through with actions required to close Change Controls
- Participate in Internal, Customer and Regulatory Audits.
- Assist with the training of new compounders
- Perform start-up and shutdown procedures for all vessels
- Minor repairs to the facility and equipment where applicable
- Perform verification checks for equipment (scales, mixers, pH meters) used in manufacturing as per predefined time periods
- May be required to assist Validation or Pharmaceutical Technology staff with new formulations and scale ups
- May be required to assist with investigations where necessary
- Notify compounding lead hand and mechanic in a timely manner if equipment parts and compounding consumables are low in quantity
- Other duties as assigned.
Knowledge, Skills and Abilities:
- Excellent math skills
- Proficient in MS Word, Excel, Powerpoint and Lotus Notes. Must be comfortable with use of tablets and trainable on associated programs (MES, SAP)
- Excellent verbal communication skills for interacting with personnel on a daily basis
- Previous experience in a pharmaceutical manufacturing environment
Background and Experience:
- University degree with 1-2 years of technical training experience
- Post Secondary education in scientific discipline is preferred or a minimum of 5 years experience in a pharmaceutical environment
- Must possess the ability to function effectively in a team environment
- Must be able to actively listen and receive coaching and applicable training
- FL licence preferred
Problem Solving:
- Issues that may arise that have a GMP impact are evaluated at the time of occurrence in conjunction with the supervisor and QA.
Working Conditions:
- Overtime will be required to address priority items. This may be additional time during the work week and / or on weekends with last minute notice
- Shift work required which may include weekends
- Physically fit, able to lift at least 25 kgs
- Stand for long periods of time
- Bending and “squatting” throughout the work day
- Use of G.M.P garments and Safety Equipment (PPE) as required
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