Compliance Manager at CATALENT CTS SINGAPORE PRIVATE LIMITED

Strathroy-Caradoc, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

03 Apr, 26

Salary

115000.0

Posted On

03 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Compliance Management, Quality Systems, Regulatory Audits, Customer Complaint Investigations, Process Improvement, Training Administration, Analytical Skills, Leadership, Communication Skills, GMP Standards, Problem Solving, Multi-tasking, Project Management, Team Leadership, Attention to Detail, Manufacturing Experience

Industry

Pharmaceutical Manufacturing

Description

Compliance Manager Position Summary Work Schedule: Regular working hours: 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch This position is 100% on-site at the Strathroy site. This position is located in Strathroy, Ontario, 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. Reporting to the Associate Director, Compliance, the Compliance Manager is accountable for the management, monitoring, improvement, and development of the following Quality Systems and programs that are applicable to the Strathroy and Windsor Compliance Program, Commercial Product Stability, Annual Product Quality Review, Customer Complaint Investigations, Training, and Strathroy site Audit Management. The Compliance Manager will ensure continuing adherence to regulatory and customer cGMP standards and foster a culture of continuous improvement within the Quality System to address changes in Regulatory expectations and landscape. The Role: Host and directly manage Regulatory, Customer and Corporate audits at the Strathroy site. Prepare and facilitate responses to the observations arising from these audits and manage the follow up and closure of the corrective actions. Manage the Commercial Stability Program, ensuring compliant and efficient preparation of protocols, pulls of samples, execution of testing, investigations of OOS’s, and preparation and approval of reports to support shelf-life expectations and resulting shelf-life assignment decisions by the Customer/Client for Catalent manufactured products. Manage the Customer Complaint Investigation process, ensuring that the system functions to identify, prioritize, and quantitate the most significant product quality issues resulting in customer complaints and rejections. Establish and lead the company process improvement teams to address the product and process quality issues that have been identified. Provide oversight for the Annual Product Quality Review program ensuring deliverables are on time and value added from a process knowledge and control perspective. Manage the Ontario Training program administration. Develop and maintain metrics to measure effectiveness of key Quality KPIs. Must be able to work extended hours, weekends as needed, especially when problems occur or when deadlines must be met Performs other duties as assigned. The Candidate: Bachelor’s degree in relevant scientific or engineering discipline is required 3+ years of management experience in the pharmaceutical industry required; experience in manufacturing or GMP environments is a plus. Knowledge and experience in dosage forms involving gelatine encapsulation is a definite asset. Understanding of the overall business needs and objectives. Excellent verbal and written communication skills. Direct experience hosting and leading the preparation, management, and follow-up relating to FDA and Health Canada inspections. Ability to multi-task, prioritize and respond quickly to a changing regulatory environment. Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience. Currently Catalent does not participate in the Ontario Immigrant Nominee Program (OINP). Candidates with non-Canadian credentials must provide an evaluation confirming the Canadian equivalency of the credentials as determined by the Alliance of Credential Evaluation Services of Canada (ACESC) such as WES. The employee's role frequently involves sitting and utilizing hands and fingers for tasks such as handling, feeling, and keyboard manipulation, necessitating manual dexterity. Occasionally, the position requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, alongside close vision capabilities and potential exposure to chemicals. Pay: The anticipated salary range for this position in Ontario is $90,000 - $115,000/Annum. The final salary offered to a successful candidate may vary within this range $90,000 - $115,000/Annum, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a global employer, and this salary range does not reflect positions that work in other countries. Why You Should Join Catalent: Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance) Group Retirement Savings –Registered Pension Plan (RPP) with employer contributions. Employee Reward & Recognition programs. Opportunities for professional and personal development & growth including tuition reimbursement. 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. 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 DisabilityAccommodations@catalent.com. 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. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The Compliance Manager is responsible for managing and improving Quality Systems and programs, ensuring adherence to regulatory standards. They will also host and manage audits, oversee the Commercial Stability Program, and lead process improvement teams.