Manufacturing Operator - hiring multiple positions!

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 Manufacturing Operator is responsible for performing all manufacturing processes related to Ocular Therapeutix’s products. The Operator is an integral part of our team and will be responsible for manufacturing activities by following appropriate SOPs and supervisor direction, in accordance with current good manufacturing practices and company policy and procedures. Ocular Therapeutix is currently hiring for several Manufacturing Operators at various levels. Compensation will vary depending upon applicable skills and experience. We provide training, a supportive environment, opportunities for advancement, strong employee benefits, and the opportunity to work in a rewarding career where you will directly be impacting patient lives! This is a full-time position based onsite Monday - Friday in Bedford, MA. Principal Duties and Responsibilities : • Perform various manufacturing processes by following documented SOPs 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 • Operates laboratory instruments such as balances, pH meters, conductivity meters, mixers, etc. • Complete documentation (batch records, process routers, forms, etc.) as required throughout the manufacturing process • Execution of routine commercial or clinical production operations. Apply GMP and GDP guidelines to all activities • Work in an environmentally controlled area (ECA) as required • Keep manufacturing areas orderly and clean according to associated SOPs. Maintain gowning area, process area and stocking production area with supplies • Troubleshoot minor issues as they arise related to equipment and/or manufacturing processes • Carry out work in a safe manner, notifying management of safety issues and risks • Reports procedural deviations and nonconformance to management • Interact with the cross functional teams including Quality Control department for the planning of testing, sample submission and monitoring activities • Maintains current training on all assigned procedures to include read & understood, skills development and classroom training activities as required • Perform other duties as required Requirements : • High-school education or equivalent required; Associate degree or biotechnology certificate strongly preferred • 1+ years related experience in a cGMP manufacturing environment • Clean room experience is preferred 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, ac