Quality Control Analyst Contract

2 weeks ago

Brampton, Canada Taro Pharmaceuticals INC, Canada Full time

**Title**:Quality Control Analyst Contract**:

- Date: Jan 10, 2023- Location: Taro Pharmaceauticals CAN- Company: Taro Pharmaceuticals INC, CanadaTaro Pharmaceuticals is a multinational, specialty pharmaceutical company with a vision of reaching people and touching lives globally as a leading provider of valued medicines. We are dedicated to meeting the needs of our customers and the overall community through the innovation, development, manufacturing and marketing of the highest quality healthcare products.

Established in 1950, Taro’s world class production facility is located in Brampton, Ontario, with a current team of over 600 Canadian employees. Our company’s focus on the dermatology sector has made us a leading manufacturer and supplier of specialized topical products with a diverse portfolio of creams, ointments, liquids, and gels.

With support from our parent company, Sun Pharma, one of the world’s largest specialty generic pharmaceutical companies, we are committed to providing a healthy, safe and rewarding environment for all of our employees.

**What we offer**:

- A safe and clean; GMP regulated work environment
- Opportunities for career growth and development
- A competitive wage/salary
- Incentive bonus programs that are designed to reward employees for their individual contributions
- Benefit programs designed to support our employees and their families, including a comprehensive health & dental benefits package, group RRSP matching program, direct access to healthcare and well-being programs, and paid time off
- Employee training and organizational development programs including tuition reimbursement, internal mobility programs, and employee recognition programs
- **10% Night Shift Premium to Base Pay**

**General Summary**:
The main responsibility of this position is to generate accurate results while following GMP requirements. Responsible for analyzing laboratory samples using various chemical and instrumental techniques, in accordance with established compendial and in-house testing methods, while under minimum supervision.

**Principal Duties and Responsibilities**:

- Testing of in-process, bulk, finished product, stability samples and raw materials by TLC, UV, IR, HPLC and GC and wet chemistry techniques as per SOP.
- Document test results as per SOP and GMP
- Recognizes OOS or out of trend results and under the direction of the Supervisor assists in the completion of lab investigations
- Interpret data, communicate results and complete written reports
- Complete all GMP documentation correctly and in a timely manner
- Complete all training assignments and maintain personal training records
- Conduct (participate or lead) routine laboratory and Non-Conformance Investigations
- Initiate and follow through with actions required to close Change Controls
- Evaluate methods and procedures and suggest improvements and changes as required
- Disposes of waste solvents and orders any chemicals or laboratory supplies as required
- Flexibility to shift start time and occasional overtime
- Other duties as assigned

**Knowledge, Skills and Abilities**:

- Proficiency in various techniques and operation of instrumentation (pH meter, viscometer, Karl Fisher apparatus, UV IR spectrophotometer, Chromatography instruments)
- Ability to work effectively in a team-based environment
- Proficiency with applicable software (LIMs and Empower)
- Strong organizational, analytical and multi-tasking ability
- Ability to troubleshoot and resolve issues
- Excellent written and oral communication skills, particularly with analytical records, reports and investigations
- Understanding of GMP’s

**Background and Experience**:

- B. Sc. or equivalent
- Minimum 1 - 3 years experience in Pharmaceutical Laboratory environment preferred

**Problem Solving**:

- Routine problems and decisions.

**Working Conditions**:

- Generally, fairly pleasant surroundings. Occasional exposure to higher than normal noise levels, frequent exposure to various chemicals used in the testing of raw materials, components and finished products. Occasional exposure to unpleasant odors resulting from testing procedures. Fairly level temperatures. Mixture of standing and walking, some light lifting and/or moving of instruments with the aid of a cart.

We thank all applicants, but only those selected for further consideration will be contacted. No phone calls please.

This position is open to applicants legally authorized to work in Canada.

Taro Pharmaceuticals embraces diversity in the workplace and is committed to achieving employment equity.

Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We ensure that our recruitment practices are supportive of this commitment and do not infringe on any characteristics protected by law.

In accordance with the Accessibility for Ontarians with Disabilities Act, 2005, and the

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