Compounding Lead

2 months ago

Brampton, Canada Taro Pharmaceuticals INC, Canada Full time

**Title**:Compounding Lead**:

- Date: Apr 23, 2024- 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

**Compounding Lead Hand**

**General Summary**:
The compounding Lead Hand co-ordinates and monitors the operation of manufacturing, ensuring the highest possible product quality is maintained, while operating in a safe and efficient manner.

**Principal Duties and Responsibilities**:

- Perform all compounding duties and responsibilities (see compounding job description)
- Ensure compliance with cGMP guidelines and SOPs maintaining a high standard of housekeeping and maintaining the daily compounding schedule
- Review batch records and other product documents as required
- Participate in scheduling activities with other members of operations and support departments as requested
- Ensure that equipment and facilities are in good condition, submit work orders for corrective action when required
- Ensure that all SOPs applicable/relating to compounding are current and that all staff are trained in their use.
- Lead staff in a safe environment making sure that safety procedures are followed at all times.
- Develop and or assist with continuous improvement projects/processes
- Investigate in-process, product and equipment failures and write reports when required
- Perform cycle counts
- Prepare batch documents when required
- Maintain inventory of miscellaneous supplies and parts
- Perform verification of equipment when required
- Participate in supervisors inter-departmental meetings when required
- Participate and conduct training sessions when required
- Provide coaching and recognition/correction to team members. Document performance of team members in a timely manner
- Treat all members fairly, without special privileges
- Lead by example and operate under ethical standards

**Knowledge, Skills and Abilities**:

- Knowledge of pharmaceutical manufacturing processes and equipment
- Excellent written and verbal communication skills, ability to communicate and work effectively in a team-based environment.
- Self motivated with a positive outlook
- Able to train and motivate team members.
- Attentive to detail with excellent organizational ability.
- Mathematical, scientific, and mechanical aptitudes.
- Excellent problem-solver with the ability to identify the root cause and make recommendations.
- Computer proficiency (MS Word, Excel, PowerPoint and Lotus Notes) combined with working knowledge of BCPS or other MRP program.
- Strong understanding of current Good Manufacturing Practices (G.M.P.) requirements.

**Problem Solving**:

- Issues may include:

- Equipment malfunction
- Ensuring consistent product quality
- Manpower and equipment “bottlenecks”
- Resolving departmental issues, while maintaining department goals. The lead hand must be resourceful and identify available resources to help or assist in dealing with the issue/problem. Resources may include Compounding Manager, QC, Technical Services, SOPs, APR etc

**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 FL licence preferred**Working Conditions**:

- May be contacted through telephone during off regular hours regarding “urg

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