Operation Shift Supervisor jobs at Amneal Pharmaceuticals - 180 jobs

A leading pharmaceutical company in Boston is seeking an experienced Associate Director to lead training initiatives within the Oncology team. The role involves developing comprehensive training programs and collaborating with sales leaders to enhance team capabilities. Candidates should have a strong background in pharmaceutical sales, preferably in oncology, along with leadership and project management skills. This position offers a competitive salary and a hybrid work environment. #J-18808-Ljbffr

A global pharmaceutical company is seeking a finance professional to contribute to the Global Finance function, supporting senior executives while managing key stakeholders. The ideal candidate will have a strong background in finance, including an MBA and extensive experience across global organizations. Responsibilities include developing finance strategies, maintaining internal and external relationships, and leading teams. Competitive compensation and benefits are offered, making this an attractive opportunity for qualified candidates. #J-18808-Ljbffr

A leading pharmaceutical company is seeking an Associate Director to define and lead global regulatory strategies. This role requires significant experience in regulatory affairs and offers opportunities for strategic leadership across multiple projects. Located in Boston, MA, the position is hybrid and provides a competitive salary range of $153,600 to $241,340. Ideal candidates will demonstrate strong communication skills and a solid understanding of drug development processes. #J-18808-Ljbffr

A leading biopharmaceutical company in Boston seeks an Associate Director for External Scientific Partnerships. This position drives strategic engagement with health professionals and organizations in the rare disease sector. Candidates should have a PhD or equivalent, alongside 3-5 years of relevant experience, strong leadership, negotiation, and project management skills. The role offers competitive pay, benefits, and a commitment to an inclusive workplace. #J-18808-Ljbffr

A leading pharmaceutical company is seeking an Associate Director for External Scientific Partnerships to develop strategic initiatives with health professional societies. The ideal candidate should hold a PhD, PharmD, or equivalent and have 3-5 years of experience in the pharmaceutical field, particularly in rare disease. This role entails fostering key partnerships and engaging with thought leaders to advance medical strategies. Competitive compensation and benefits are offered, including an annual salary ranging from $150,202 to $225,304. #J-18808-Ljbffr

A global pharmaceutical company is seeking a Senior Vice President of Patient and Market Access to optimize access to innovative therapies. The role involves leading strategies for reimbursement, directing a team to achieve performance goals, and engaging with healthcare stakeholders. The ideal candidate brings 20+ years in the pharmaceutical industry, including extensive experience in Market Access and a deep understanding of the US healthcare system. A commitment to fostering an inclusive team environment is essential. #J-18808-Ljbffr

A global healthcare leader in San Francisco is seeking an Associate Director for their External Partnering team. This role focuses on driving molecule discovery and technology licensing, enhancing portfolio growth through new business opportunities. Candidates should possess deep knowledge in drug discovery, a minimum of 7 years experience in client services or sales within pharmaceutical environments, and strong relationship-building skills. Competitive salary range of $132,000 - $193,600 offered, alongside comprehensive benefits. #J-18808-Ljbffr

A global biotechnology company is seeking a Principal Research Scientist in San Diego to focus on targeted drug delivery, particularly nucleic acid therapies. The ideal candidate will have expertise in receptor biology, collaborate with cross-functional teams, and contribute to innovative therapeutic programs. A Ph.D. or equivalent in biology or a related field is required, along with relevant experience of 4-10 years depending on the educational background. #J-18808-Ljbffr

A leading biopharmaceutical company is seeking an Associate Director to serve as Regional Regulatory Lead, overseeing complex regulatory submissions and managing cross-functional teams. The ideal candidate should have significant regulatory experience, a strong track record in strategy development, and excellent negotiation skills. This role offers a chance to influence drug development processes in a dynamic environment. #J-18808-Ljbffr

A leading biopharmaceutical company in California seeks an Associate Director in CMC Regulatory Affairs to lead regulatory strategy and ensure compliance in biologics development. The ideal candidate will have over 10 years of experience and proven success in executing CMC strategies. Strong leadership and communication skills are essential. Competitive salary range is $182,070.00 to $235,620.00 with comprehensive benefits. #J-18808-Ljbffr

A leading biotechnology firm is seeking a Clinical Imaging Scientific Director for Oncology to lead imaging strategy and execution in clinical trials. The ideal candidate will have a PhD and over 10 years of experience in clinical imaging, particularly in oncology, with significant expertise in PET imaging and regulatory engagement. This role requires collaboration with research teams and overseeing imaging project implementation, contributing significantly to oncology drug development. Comprehensive benefits are offered to eligible employees. #J-18808-Ljbffr

A leading biotechnology firm is seeking a Clinical Imaging Scientific Director for Oncology to lead imaging strategy and execution in clinical trials. The ideal candidate will have a PhD and over 10 years of experience in clinical imaging, particularly in oncology, with significant expertise in PET imaging and regulatory engagement. This role requires collaboration with research teams and overseeing imaging project implementation, contributing significantly to oncology drug development. Comprehensive benefits are offered to eligible employees. #J-18808-Ljbffr

A biopharmaceutical company is seeking a Senior Manager for Global Regulatory Affairs in Oncology. This role involves acting as the Regional Regulatory Lead, defining regulatory strategies for multiple products, and representing the company in negotiations with regulatory authorities. The ideal candidate will possess significant regulatory experience in the biopharma sector and proven leadership skills. This position is remote and full-time, primarily based in the United Kingdom. #J-18808-Ljbffr

A leading biopharma company in California seeks an Associate Director of Regulatory Affairs - Global Labeling. The ideal candidate will lead labeling strategies and manage regulatory negotiations. Candidates should possess a PharmD/PhD or a BA/BS with extensive relevant experience in regulatory affairs. This position involves strategic oversight across multiple therapeutic areas, emphasizing compliance and collaboration with various stakeholders. #J-18808-Ljbffr

A global biopharmaceutical company in Foster City is seeking a Director, Global Pricing & Analytics Lead to oversee pricing and analytics for its LIVE portfolio. The ideal candidate will have a strong background in strategic pricing, market access, and health economics, along with leadership skills to manage cross-functional teams. This role requires expertise in pricing governance and analytics to drive decision-making and support product launches. #J-18808-Ljbffr

A leading biopharmaceutical company seeks an experienced professional to oversee digital modernization of CMC RA platforms in Foster City, California. The role requires strong experience in regulatory operations, strategic planning, and change leadership, along with a PhD or MS in chemistry or related fields. The successful candidate will lead workforce capability design and create processes for knowledge management in alignment with strategic priorities. #J-18808-Ljbffr

A leading biopharmaceutical company is seeking an Executive Director for Global Value and Access in HIV. The role involves developing and executing strategies to enhance value and access for Gilead's HIV portfolio. Candidates should have extensive experience in the biotech or pharmaceutical industry and strong leadership skills. This is a full-time position based in California with a focus on innovation and inclusion. #J-18808-Ljbffr

Our Supervisor, Manufacturing Operations (Formulation) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you will be responsible for daily coordination and working schedules of people and equipment in Formulation Operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role for our 2nd shift, working Monday through Friday from 2PM to 10:30PM. This is a set, consistent schedule based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the Supervisor, Manufacturing Operations (Formulation) Does Each Day: Runs operation to meet or exceed delivery performance objectives for product or projects Supervises staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedback Counsels, trains, & develops technicians for efficient performance; creates an atmosphere of team effort & open communication Completes in-process checks & verifications in alignment with Standard Operating Procedures Reviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices Develops technician training programs & assures operator training is conducted Troubleshoots or resolves issues impeding daily/weekly deliverables; proactively demonstrates the ownership to achieve Reviews operational performance and drives improvement opportunities Initiates & executes change control assignments in support of continuous improvement initiatives for equipment, documentation, or processes Drives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closure Reports & initiates production schedule changes, requests equipment and facility repairs, or modifications Our Most Successful Supervisor, Manufacturing Operations (Formulation): Meets productivity standards; Completes work in timely manner; Strives to increase productivity Follows policies and procedures; completes administrative tasks correctly and on time Prioritizes and plans work activities; Sets goals and objectives; Organizes or schedules other people and their tasks Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments Minimum Requirements for this Role: High school Diploma or GED from recognized institution or organization required 2-3 years prior experience in cGMP / FDA regulated industry 1 year of supervisory or management experience required Successful completion of certified in-house qualification programs Experience training personnel on aseptic techniques and appropriate gowning techniques Well versed in the compliance & quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolution Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Any of the Following Will Give You an Edge: Bachelor's Degree in Life Science or another related field Computer Skills Training Software Microsoft Suite ERP software Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 22 paid days off plus 8 paid holidays per year National, industry-leading high growth company with future career advancement opportunities The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions Range: $65,023- $89,047 Annually About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

PL Developments, also known as PLD, is a leading manufacturing, packager and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. We are seeking a Warehouse Operator to join our team. The ideal candidate will be responsible for efficiently performing a variety of tasks within the warehouse, including order picking, receiving, shipping, inventory management, and operating warehouse equipment such as forklifts. This role involves ensuring accuracy in all tasks, adhering to safety and quality standards, and maintaining a clean and organized work environment. Work schedule: Monday - Friday: 9:00 AM - 5:30PM JOB QUALIFICATIONS: High School Diploma or GED 1 - 3 years internal and/or 3+ years external warehouse experience required Must be able to operate a single, deep reach truck, counter-balanced forklift, rider, order picker and swing reach lift. As applicable per site. Excellent math, analytical skills, and attention to detail Detail oriented with good organization and communication skills Self-starter with the ability to meet internal company goals Demonstrates reliability and responsibility Willing to learn, must have a flexible availability Ability to work effectively individually and/or a part of a team Able to meet and/or exceed performance standards POSITION RESPONSIBILITIES: Proficient on WMS manual Able to perform the core tasks of sales order picking, work order picking, purchase order receiving, as applicable per site. Shipping Tasks, ability to execute replenishment, consolidation, checking, running pallets, loading, and any other shipping related tasks. Receiving Tasks, ability to execute unloading, cycle counts, putaways, and any other receiving and/or inventory related tasks. Utilize Oracle desktop forms Ability to unload and putaway pallets from automation equipment as applicable per site. Report damage of product, storage racks, forklifts, warehouse equipment, or any unsafe condition to management immediately Follow all Safety and cGMP guidelines Ability to verify that their work is accurate and complete Verify safety inspection sheet and/or iWarehouse checklist has been completed before operating a forklift Operate a forklift in a safe and efficient manner to retrieve or store material Always maintain work area clean, orderly, and inspection ready. This includes but is not limited to emptying trash cans, trash bins, sweeping, mopping, dusting racks, dock doors and other duties as assigned by supervisors or managers. PHYSICAL REQUIREMENTS: Employees in this class are subject to extended periods of sitting, standing, walking, pushing and pulling, stooping and crouching and climbing. Occasional lifting of equipment or materials weighing up to 80 pounds. Employees must wear proper PPE as required when handling different materials and operating equipment. Hourly rate: $18.00 - $20.00/hr PLD is a proud equal opportunity employer offering many corporate benefits, including: Medical and Detal Benefits 401k with employer match Group Life Insurance Flex Spending Accounts Paid Time Off and Paid Holidays Tuition Assistance Corporate Discount Program Opportunities to Flourish Within the Company PL Developments is an Equal Opportunity Employer. All qualifies applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.