Controls Engineer

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a pioneering biopharmaceutical company dedicated to the formulation, development, and commercialization of groundbreaking therapies for eye diseases and conditions, utilizing our innovative bioresorbable hydrogel-based formulation technology, ELUTYX™. With a robust pipeline of drug delivery solutions, we aim to simplify and enhance the current standard of care, positioning ourselves as a leader in the ophthalmic industry.At our Bedford, MA headquarters, we foster a vibrant culture that encourages employees to grow and achieve their career aspirations. We promote innovative thinking, cross-functional collaboration, and creativity.Position SummaryThe Quality Control Analyst, Data Review, plays a crucial role in ensuring the integrity of analytical chemistry and microbiology data for small-molecule and combination products. This position is essential for maintaining accurate and compliant electronic and paper QC records according to cGMP, GLP, and ALCOA+ data integrity standards, supporting batch release, stability programs, environmental monitoring, method validation, device testing, and regulatory submissions.

Ocular Therapeutix, Inc. is hiring a Quality Control Analyst I for the Raw Materials team in Bedford, MA. This position helps ensure the quality and safety of materials used in the company’s ocular therapeutics products. Role overview The Quality Control Analyst I focuses on testing and analyzing raw materials. Attention to detail and accuracy are important in this work, as results support the company’s commitment to high standards. Key responsibilities Conduct analyses of raw materials according to established procedures Maintain clear and accurate documentation of test results Collaborate with cross-functional teams to support quality objectives Requirements This role requires dedication to quality and the ability to work effectively within a team. Experience in laboratory analysis and documentation is important.

Join Ocular Therapeutix, Inc. as a Principal Quality Control Analyst specializing in Microbiology. In this pivotal role, you will lead quality control initiatives, ensuring the highest standards in microbiological testing and compliance within our manufacturing processes. Your expertise will drive continuous improvement in our quality systems, ultimately enhancing patient safety and product integrity.As part of our dynamic team, you will collaborate with cross-functional departments to implement quality assurance protocols, conduct audits, and provide training on microbiological best practices. Your contributions will be vital in maintaining our commitment to excellence in the pharmaceutical industry.

Join our dedicated team at AWP Safety as a Traffic Control Flagger, where your role will be vital in ensuring the safety of both workers and the public in construction zones. As a key member of our traffic management team, you will be responsible for directing vehicle and pedestrian traffic, setting up traffic control devices, and communicating effectively with motorists and pedestrians. Your vigilance and commitment to safety will help create a secure environment on the job site.

As an Assistant Controller at Ocular Therapeutix, you will play a pivotal role in overseeing financial operations and ensuring compliance with accounting standards. You will assist in the preparation of financial statements, manage accounting records, and support the Controller in strategic financial planning. This position demands attention to detail, analytical skills, and a strong understanding of financial regulations.

Ocular Therapeutix, Inc. develops and commercializes therapies for eye diseases, using its proprietary ELUTYX™ hydrogel-based technology. The company’s Bedford, MA headquarters fosters a collaborative and creative workplace, where new ideas and teamwork are valued. Role overview The Quality Assurance Compliance Manager oversees and improves key quality assurance activities, ensuring that the organization’s processes align with regulatory standards and support GxP operations. Main responsibilities Manage Supplier Quality, including audits, documentation, training, inspection readiness, and ongoing compliance with regulatory requirements. Prepare the site for both internal and external audits, confirming that systems and processes meet regulatory expectations. Lead vendor audit coordination and manage the qualification process for vendors involved in GxP activities, including vendor selection and risk assessments. Work with cross-functional teams on vendor onboarding, resolve Supplier Corrective Action Requests (SCARs), and evaluate Supplier Change Notifications (SCNs). Support the Quality Organization by managing deviations, change controls, and Corrective and Preventive Actions (CAPAs). Review and assess departmental documentation, such as Standard Operating Procedures and Work Instructions, to identify gaps and suggest improvements. Maintain compliance with all company policies, procedures, and GxP guidelines, while seeking opportunities to enhance and streamline quality operations. Assist with the rollout and implementation of new electronic systems, including MasterControl.

Ocular Therapeutix is hiring a Quality Assurance Associate with a focus on Records Management in Bedford, MA. This position supports the company's commitment to maintaining high quality standards and meeting regulatory requirements. Role overview The Quality Assurance Associate will help manage records that document compliance and quality processes. This work ensures therapies meet safety and regulatory expectations, supporting the company's mission to improve patient outcomes. Key responsibilities Maintain and organize quality records to support compliance efforts Assist in upholding quality standards for therapies Contribute to documentation that demonstrates adherence to safety and regulatory guidelines Impact This role directly supports the delivery of safe therapies by ensuring accurate and complete records. The work helps the organization meet regulatory expectations and contributes to better outcomes for patients.

Ultragenyx Pharmaceutical Inc. seeks a Senior Specialist, Quality Assurance Operations, to help maintain quality and compliance for drug substance manufacturing. This role is essential in supporting the production of therapies that meet regulatory and company standards. Schedule and Location This position is based on-site in Bedford, MA. The regular work schedule is Sunday through Wednesday, from 7 AM to 5:30 PM. Key Responsibilities Ensure products meet established quality and compliance requirements throughout the development and production process. Collaborate with a team focused on upholding high standards in drug substance operations.

Why Choose Us? Become a champion for patients with rare diseases. At Ultragenyx, we firmly believe that making a genuine impact on the lives of patients and our team is always the right path to take. Our vision is to pioneer the future of rare disease medicine. This means venturing where other biopharma companies hesitate—defying the norm and forming a new paradigm that propels our industry forward so that more patients and caregivers can access transformative treatments. We achieve this through a commitment to scientific integrity, a unique rapid development methodology, producing innovative medications at fair prices, and fostering a collaborative environment that connects with patients in meaningful ways. Our dedication to patient care extends to our workforce, making culture a vital pillar at Ultragenyx. We are relentlessly focused on cultivating a supportive and inclusive environment rich in learning and growth, allowing employees to flourish both personally and professionally. Ultimately, we aspire to be an organization where we would be proud for our family and friends to join. If you are eager to make a significant impact, excel in your career, and experience substantial personal and professional growth, we invite you to join our team.Position Overview:Ultra-focused – Collaborate to boldly explore new horizons.Ultragenyx is in search of a seasoned Senior Director of Supply Chain Quality to spearhead global quality leadership and oversight across packaging, labeling, global supply chain operations, and quality systems. This role will be pivotal in ensuring the integrity of our supply chain processes, ultimately benefiting our patients and stakeholders.

Join Our Team as a Board Certified Behavior Analyst (BCBA)Are you a passionate and dedicated BCBA looking for a rewarding role? At ABA Centers of America, we offer a collaborative and supportive environment designed to help you thrive.Compensation: $95,000 - $115,000 annuallyExciting Benefits:Relocation Package up to $15,000Student Loan Forgiveness up to $24,000Why Choose Us?At ABA Centers of America, we pride ourselves on creating an exceptional work culture for BCBAs:Manageable billable hours (27 hours/week)Smaller caseloads (8-10 cases, with 180 RBT hours/week)Flexible scheduling optionsYour Impact:As a BCBA, you will:Design, implement, and monitor treatment programs for skill acquisition and behavior reduction.Oversee RBTs and caregivers in delivering effective behavior-analytic interventions.Conduct various assessments to determine behavioral intervention needs.Actively supervise BCBA certification candidates.What We’re Looking For:We seek candidates with:Master's degree in a related fieldActive BCBA certificationInitiation of state licensure process prior to start dateValid driver's license and reliable transportation

Join our team as a Part-Time Retail Data Collection Associate, where you will play a vital role in gathering and analyzing retail data. This position is perfect for individuals looking to contribute to insightful market research and analysis in the retail sector. Your responsibilities will include visiting designated retail locations, collecting data on product placements, pricing, and promotional activities, and providing feedback to improve retail strategies.

Join our dynamic team at Integrated Resources Inc. as a Testing Assistant, where you will play a crucial role in ensuring the quality and reliability of our products. As a Testing Assistant, you will collaborate closely with our testing team to execute test plans, document results, and provide insights that drive product improvements.

Clinical Director / BCBA at ABA Centers of AmericaLocation: Bedford, NHCompensation: $125,000 - $150,000 base salaryStudent Loan Forgiveness: Up to $24,000Join Our Leadership Team!Are you a Board Certified Behavior Analyst (BCBA) seeking to elevate your career within a supportive and innovative environment? At ABA Centers of America, we prioritize the expertise of our clinical staff in decision-making processes, ensuring that your voice is not just heard but valued. As we expand our services to meet the rising demand for ABA therapy, we invite you to help shape the future of the industry.Your Role:As the Clinical Director, you will oversee the daily clinical operations of our Bedford clinic, ensuring the effective delivery of ABA therapy services. You will facilitate communication among BCBAs, RBTs, and the broader team, fostering a collaborative clinical environment.Key Responsibilities:Lead and manage a team of BCBAs and RBTs to maintain high clinical standardsSupervise the execution of behavior intervention strategies, treatment plans, and client documentationMentor and provide professional development opportunities for BCBAsConduct assessments and develop treatment plans for new clients as requiredSupport extended assessment processes (FBA, FA, preference assessments, etc.)Review client progress through weekly meetings with BCBAsProvide on-site supervision and support for clinical staffMaintain regular communication with families through monthly check-insContribute to the ABA Academy of Excellence training program by analyzing data to enhance treatment integrityCollaborate with the Regional Operations team to develop and implement clinic-focused curriculaSupervise unrestricted hours for BCBA Apprentices, ensuring compliance with training requirementsTravel as needed for assessments and to support high-risk clientsWhy Choose Us?Commitment to Exceptional Outcomes: Our smaller caseloads and established clinical infrastructure empower you to deliver impactful, high-quality care to children and families.AI-Driven Workflows: We leverage technology to streamline administrative tasks, allowing you to devote more time to client care.Unlimited Career Advancement: Experience long-term growth opportunities without the constraints of private equity pressure.Mentorship and Leadership Development: Work alongside seasoned BCBAs and leaders dedicated to your professional growth.Special Interest Groups: Engage with peers to expand your expertise in critical areas such as assessment and collaboration.