Technical Services Specialist Jobs

Strathroy, Ontario is one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.
Position Summary
Reporting to the Technical Services Manager, the Technical Services Specialist will lead projects in order to commercialize new products and technologies and to optimize commercial manufacturing processes. This will include activities such as process scale-up (pertaining to both products and technologies), technical transfers, commercialization, and ongoing product/process stewardship. This will be accomplished by focusing or product/process robustness, quality. customer service and cost performance. The Technical Services Specialist will have an introductory knowledge of various aspects of implementing the drug development process in a regulated environment, including topics such as Quality by Design (QbD), Design of Experiment (DOE) and compliance with regulatory guidelines.
The Role

• Must be able to work extended hours. weekends as needed, especially when problems occur or when deadlines must be met
• With R & D. QA and Operations, participate in the evaluation and risk assessment of project/program data in order to implement products and technologies into commercial production; establish process improvement based on trend analysis and study data; investigate issues and customer complaints and determine corrective actions: and ensure commercial product manufacturing processes are robust.
• Operate under and maintain GMP/GLP conditions.
• In collaboration with R & D, QA and Operations, plan, coordinate, and drive assigned projects by workings with staff and Project Management. within the Catalent Project Management framework, to ensure timelines are met, roadblocks are identified early, and resources are coordinated.
• Perform other duties as required
• Prepare and execute process validation protocols, process validation reports, study protocols and reports as appropriate.
• Effectively communicate in a timely manner with management and other departments within Catalent to ensure clear understanding and acknowledgement of project status. risks. actions and outcomes.
• Represent department on a technical basis for assigned projects at local meetings.

The Candidate

• Bachelor's Degree in Pharmacy, Science, Engineering (Chem., Indus., Mech., Elec.) or related field.
• Experience working in a manufacturing, pharmaceutical and/or GMP facility an asset
• Demonstrated ability to work independently. tic initiative and complete assigned projects independently
• Experience in study design, execution, and reporting an asset
• Good writing skills

Regular working hours: 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch
Why you should join Catalent:

• Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance).
• Opportunities for professional and personal development & growth incl. tuition reimbursement
• Employee Reward & Recognition programs.
• Paid Time Off Programs incl. vacation, banked time & personal time.
• Group Retirement Savings –Registered Pension Plan (RPP) with employer contributions.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone’s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.