Senior Regulatory Affairs Specialist - CMC

Bausch + Lomb (NYSE / TSX : BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world from the moment of birth through every phase of life.

Our mission is simple, yet powerful : helping you see better, to live better.Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives.

Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing, and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe.

We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

ObjectivesA member of the global technical CMC team for global regulatory CMC strategy for submissions and content of CMC dossiers for prescription drugs and consumer products.

The team liaises with R&D and Quality organizations to prepare and maintain CMC sections of submissions and respond to Health Authority queries throughout the product lifecycle.

Responsible for regulatory compliance and change management. Responsible for regulatory compliance, regulatory intelligence surveillance and US regulatory licensing.

ResponsibilitiesProactively communicate CMC regulatory strategy, key issues and any other critical topics throughout the life cycle to interdisciplinary project teams and to appropriate management level in Regulatory Affairs, R&D, TechOps and Supply Chain as appropriate in a timely manner.

Lead and drive all CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects / products.

Make quality regulatory decisions, balancing risks and benefits with supervisor input.Identify, as early as possible, the required documentation and any content, quality and / or timeline issues.

Negotiate the delivery of approved technical source documents in accordance with project timeline.Coordinate with Regulatory Operations to ensure timely and accurate submissions to Regulatory Authorities.

Provide regulatory support to other company functions during Regulatory Authority inspections.Serve as Regulatory Affairs representative on facility / site Local Change Management Boards.

Review and provide input on proposed health authority guidance documents on CMC issues.Author the annual reports for all non-marketed Rx products independently.

Provide the CMC portion of Annual Product Reviews (APR’s) for a specified internal manufacturing site.Author minor (CBE0 & CBE30) CMC supplements (i.

e. spec change to align with compendia, add drug substance testing sites) with supervision.Work closely and collaborate with CMC Managers & Product Leads on international market requests.

Actively participates in team activities.Act as primary contact with regulatory authorities with limited supervision.RequirementsBachelor degree preferred or equivalentMinimum of 3 years Regulatory Affairs experience or relevant experience in a regulated environmentExcellent communication / interpersonal and writing skillsSelf-motivated and capable of working independently with minimal supervisionSkilled in basic technologies (e.

g., MS Office Applications, Adobe Acrobat, MS Project)Knowledge of country regulations (med device and pharma), post market surveillance, ISO and IECDetail oriented with the ability to proofread and check documents for accuracy and inconsistenciesCommand of English language (verbal and written)Ability to understand scientific information and assess whether technical arguments are articulated clearlyExperienced in good documentation practices and requirements for managing regulated recordsDemonstrated ability to contribute to a continuous learning and process improvement environmentSome knowledge of how create a successful product regulatory strategyOperates with a sense of urgency, agility and flexibilityWe offer competitive salary & excellent benefits including : Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date401K Plan with company match and ongoing company contributionPaid time off vacation (3 weeks - prorated upon hire), floating holidays and sick timeEmployee Stock Purchase Plan with company matchEmployee Incentive BonusTuition Reimbursement (select degrees)Ongoing performance feedback and annual compensation reviewFor U.

S. locations that require disclosure of compensation, the starting pay for this role is between $70,000 and $120,000 . The estimated salary range reflects an anticipated range for this position.

The actual base salary offered may depend on a variety of factors.U.S. based employees may be eligible for short-term and / or long-term incentives.

They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others.

U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

To learn more please read Bausch+Lomb's Job Offer Fraud Statement () .Our Benefit Programs : Applicants must be authorized to work for ANY employer in the U.

S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.