At a Glance
- Tasks: Lead and supervise manufacturing processes for innovative eye therapies.
- Company: Join a pioneering biopharmaceutical company focused on eye health.
- Benefits: Competitive salary, career growth, and a supportive work culture.
- Other info: Dynamic environment with opportunities for creativity and collaboration.
- Why this job: Make a real impact in the ophthalmic industry while developing your skills.
- Qualifications: Associate's degree required; experience in pharmaceuticals preferred.
The predicted salary is between 80000 - 85000 £ per year.
Ocular Therapeutix, Inc. (NASDAQ: OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™.
Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.
Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals.
We encourage out of the box thinking, cross-functional collaboration, and creativity.
Position Summary
The Supervisor, Manufacturing is responsible for performing and assisting with all processes related to the manufacture of Ocular Therapeutix products.
This includes the routine execution of clinical trial builds, commercial production builds and integration of new processes within the current pipeline.
Principal Duties an Responsibilities
- Lead and supervise daily manufacturing activities by scheduling tasks and roles for operators to efficiently complete manufacturing.
- Supervise manufacturing operator direct reports while addressing any concerns of team members and providing conflict resolution as necessary.
- Provide feedback throughout the year to direct reports and conduct routine performance reviews.
- Apply c GMP and c GDP guidelines to all activities.
- Perform various manufacturing processes by following documented SOP’s and procedures, calculating requirements, weighing materials, and operating various equipment.
Processes include but are not limited to formulation, inspection, in-process packaging and finished product packaging.
- Complete documentation (batch records, process routers, forms, etc.) and review of executed documentation as required throughout the manufacturing process.
- Troubleshoot issues as they arise related to equipment and/or manufacturing processes.
- Own and complete deviations and CAPAs related to the manufacturing process.
Properly identify deviations and accurately document the events.
Work cross functionally to arrive at corrective actions and implement the identified action.
- Proactively identify and implement process improvements related to a continuous effort to improve culture, repeatability, execution and compliance.
Navigate within the existing quality process to properly deliver the identified improvement.
- Train operators on new processes and ensure operators are properly trained for the task or role.
- Learn multiple product manufacturing operations and assist in the transfer of the process between manufacturing and process development.
Identify issues and solve problems relating to the implementation of a repeatable manufacturing operation.
- Assist in new process integration into the manufacturing group.
- Perform other duties as required.
Qualifications
- Associate’s degree is required, bachelor’s degree in a science field or equivalent preferred
- 2-4 years of prior experience in the pharmaceutical industry is required
- GMP clean room experience is required as well as knowledge of FDA regulations, c GMP and c GDP’s
- Chemical handling and solution preparation experience preferred
- Ability to evaluate manufacturing schedule and appropriately assign operators and roles
- Basic computer knowledge, such as Microsoft Word, Outlook and Excel is required
- Must have very good written and oral communication skills as well as willingness to learn
- Ability to interact with all Manufacturing Managers, Manufacturing Engineers, Quality Control, Research & Development and other personnel
- Excellent organizational skills and attention to detail with the ability to multitask
- Ability to work in environmentally controlled areas (ECA) or lab environment
Working Conditions
- Ability to gown and gain entry to pharmaceutical manufacturing areas; ability to wear personal protective equipment such as safety glasses/goggles, gloves, and safety shoes
- Ability to lift, pull or push equipment requiring up to 25-50 lbs.; ability to stand for 6 hours in a production suite
- Ability to climb ladders and work platforms
- Ability to work flexible hours to complete work activities
- Ability to work around chemicals (alcohols, acids & bases
- #LI-LM1
- Salary Range
- $80,000
- $85,000
- USD
Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination.
Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran.
For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www. ocutx. com/privacy-policy/ . For the Privacy Notice for California Job Applicants, please see
CCPA Applicant Notice .
Supervisor, Manufacturing in Bedford employer: Ocular Therapeutix
Ocular Therapeutix, Inc. is an exceptional employer located in Bedford, MA, where we foster a vibrant work culture that encourages innovation and collaboration. As a Supervisor in Manufacturing, you will benefit from our commitment to employee growth through continuous training and development opportunities, all while contributing to groundbreaking therapies in the ophthalmic field. Join us to be part of a team that values creativity and supports your career aspirations in a dynamic biopharmaceutical environment.
StudySmarter Expert Advice🤫
We think this is how you could land Supervisor, Manufacturing in Bedford
✨Unlock Networking Opportunities
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Ocular Therapeutix.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Ocular Therapeutix. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Ocular Therapeutix is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Supervisor, Manufacturing in Bedford
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Ocular Therapeutix!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Ocular Therapeutix that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Ocular Therapeutix!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Ocular Therapeutix, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Ocular Therapeutix
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Ocular Therapeutix that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Ocular Therapeutix’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
