Ocular Therapeutix

Supervisor, Manufacturing

Ocular Therapeutix • $80K — $85K *
Bedford, MA 01730In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Associate's degree required; Bachelor's in a science field preferred.
  • 2-4 years of experience in the pharmaceutical industry required.
  • Experience in GMP clean rooms and knowledge of FDA regulations, cGMP and cGDP.
  • Preferred experience with chemical handling and solution preparation.
  • Strong written and oral communication skills, with a propensity for learning.
  • Basic proficiency in Microsoft Word, Outlook, and Excel.

Responsibilities

  • Lead and schedule daily manufacturing tasks for operational efficiency.
  • Supervise and address team member concerns, ensuring a cohesive work environment.
  • Provide ongoing feedback and conduct routine performance reviews for direct reports.
  • Apply cGMP and cGDP guidelines consistently in all manufacturing activities.
  • Perform various manufacturing processes according to documented procedures and SOPs.
  • Document and review batch records and manufacturing processes diligently.
  • Troubleshoot equipment and manufacturing issues promptly.

Benefits

  • Opportunity for career growth within a specialized field.
  • Training in new processes and cross-functional integration.
  • Engagement in continuous improvement initiatives for company culture.
  • Exposure to cutting-edge ocular therapeutic technologies.
  • Comprehensive training programs to enhance operational competencies.
Full Job Description
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 cGMP and cGDP 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, cGMP and cGDP'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


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Salary Range

$80,000-$85,000 USD

About Ocular Therapeutix

Ocular Therapeutix is a biopharmaceutical company that develops and commercializes therapies for diseases and conditions of the eye. The company's lead product candidate, DEXTENZA, is a corticosteroid that is used to treat post-surgical ocular inflammation and pain. Ocular Therapeutix was founded in 2006 and is headquartered in Bedford, Massachusetts. The company is publicly traded on the NASDAQ under the ticker symbol OCUL.
Learn more about Ocular Therapeutix
Size
228 employees
Market Cap
$210.9 million
Industry
Pharmaceuticals & Biotech
Net Income
-$155.6 million
Founded
2006
5 Year Trend
+87.3%
Revenue
$17.4 million
NASDAQ
OCUL
* Ladders Estimates

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