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Manufacturer of nutritional supplements, bars and protein powders. Responsibilities: Install, set up, configure, maintain and repair processing and packaging equipment in accordance with production requirements and scheduling with the ultimate goal of reducing equipment downtime. Receive daily work schedule from the Maintenance Supervisor, prioritize assigned duties and take required actions to ensure dependable and functional operation of machinery equipment. Fillers, hoppers, cappers,....


Manufacturer of nutritional supplements, bars and protein powders. Responsibilities: Install, set up, configure, maintain and repair processing and packaging equipment in accordance with production requirements and scheduling with the ultimate goal of reducing equipment downtime. Receive daily work schedule from the Maintenance Supervisor, prioritize assigned duties and take required actions to ensure dependable and functional operation of machinery equipment. Fillers, hoppers, cappers,....


Manufacturer of nutritional supplements, bars and protein powders. Responsibilities: Install, set up, configure, maintain and repair processing and packaging equipment in accordance with production requirements and scheduling with the ultimate goal of reducing equipment downtime. Receive daily work schedule from the Maintenance Supervisor, prioritize assigned duties and take required actions to ensure dependable and functional operation of machinery equipment. Fillers, hoppers, cappers,....

- Rochester, MN
new job!

Our client is a high growth food production company that offers you great career progression and an excellent rewards package that includes a company match 401(k) and an annual merit increase performance review. Responsibilities:Assess and update quality systems, procedures, methods and processes for raw materials and processed productsEnsure conformance to all requirements of the Quality Management System for SQF 2000 certificationEnforce safety rules and practices, safe work behaviors,....


Join a global leader as Corporate Facilities and Services Manager with multi site responsibility including admin buildings, laboratories, horticulture, greenhouses, HSE and contract services. Offers excellent benefits including salary, bonus, and relocation package. Requirements: --- Bachelor degree with 10+ years experience in the area of facilities / buildings management in a commercial and/ or R&D environment (includes office buildings, utilities, laboratories, horticulture,....


Global Pharmaceutical company in Madison, New Jersey is looking for a Pharmacovigilance Agreements & Alliance Management Specialist We are looking for candidates with a PharmD or RN/NP with individual case safety report processing experience and knowledge of global drug safety/PV regulations, i.e., Drug Safety Associate/Sr. Associate/Manager. I. POSITION SUMMARY: The PV Agreements & Alliance Management (PAAM) Specialist guides and facilitates effective working relationships with....

- Madison, NJ
new job!

New need for Growing Global Pharmaceutical Company in New Jersey Contract R&D Project Planner III This R&D Project Planner is responsible for supporting Clinical Trial/Project Teams by strategically developing and maintaining clinical study timelines, providing evaluations of potential risks and conflicts, supporting the team on proactively resolving potential deviations, and presenting clear timeline reports. PP will work in a team orientated environment and is empowered to drive....

- Madison, NJ
new job!

Global Pharmaceutical company is expanding in new offices in Madison, NJ This Clinical Trial Manager is an essential part of the Clinical Operations team. Looking for a strong Clinical Trials Professional with a operation experience for phase 2, 3 and 4 trials. Multiple therapeutic reas. -responsible for the delivery of studies , responsible for the execution and adherence of various aspects of the study operational plan (start up, conduct, close-out, and vendor oversight) with input from key....

- Cambridge, MA
new job!

Publicly Traded Top Tier Global Pharmaceutical Company is looking for a Clinical Study Manager or Senior level DOE to be located in their Cambridge, MA Headquarters competitive base salary and bonus, full relocation and stock and other long term incentives! This role requires a strong communicator: Duties and Responsibilities: 1.Manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD, and ICH GCP) and Company SOPs, and supporting....


New contract role (opportunity to convert to perm in future if desired) with Global Pharmaceutical company located in Cambridge, MA BACKGROUND: This Drug Product is an ALK Inhibitor for the treatment of patients with anaplastic lymphoma kinase-positive (ALK+) metastatic NSCLC. It was recently approved by the FDA under Accelerated Approval in April 2017, based on tumor response rate and duration of response, for previously treated anaplastic lymphoma kinase-positive (ALK+) metastatic....

- New York, NY
new job!

My client seeks a Manager of Business Development to provide exceptional service to their biotechnology and pharmaceutical clients. This person will support the Director of Business Development, meet with decision makers of pharma and biotech firms, review their current R&D landscape, and offer solutions (both internal and external) to their clients. The focus of the position is to develop relationships with clients, build rapport with the R&D groups, and help the firm grow into the....

- New York, NY
new job!

My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharmaceutical and biotechnology partners and ensure quality service to Directors & VPs, Principal Investigators and other clients.Develop and expand research and clinical collaborations with new partners.Work closely with Chief Medical Officer and ensure project deliverables are met.Understand the....

- Rockville, MD
new job!

My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharmaceutical and biotechnology partners and ensure quality service to Directors & VPs, Principal Investigators and other clients.Develop and expand research and clinical collaborations with new partners.Work closely with Chief Medical Officer and ensure project deliverables are met.Understand the....

- Phoenix, AZ
new job!

My client is focused in the oncology space, and they seek a Project Manager to take on the following tasks:Support project development activities and the overall coordination of proof-of-concept, proof-of-efficacy preclinical research projects, non-clinical toxicology and pre-IND activities for internal projects.Collaborate with a cross functional team including internal scientists and CROs to prepare study designs, manage budgets to perform the studies, and oversee the study from initiation....

- Cincinnati, OH
new job!

This position provides technical leadership and accountability for computer system validation and ensures compliance with internal and external computerized system policies and regulations. As the Subject Matter Expert, this individual will ensure sites are fundamentally aware of and proactively implement current computerized system validation practices with particular focus on impact to patient safety, product quality and record integrity. Position scope includes local and global site systems


Job Description: We are seeking an experienced and determined professional with a passion for Project Management. As a consultant you will primarily work with clients in the pharmaceutical industry. You will engage directly with key decision makers and have the potential to create true impact. Tasks will mainly relate to Project Management of or within large investment projects. We are looking for a candidate with strong leadership and communication skills who is driven by a desire for....

- Chicago, IL

$25B Pharmaceutical Company—North Chicago—Salary Commensurate with Experience The SizzleCompany offers great work/life balance.Company offers competitive benefits and perks, including insurance, PTO and sick days, and work flexibility.Company prides itself on having a diverse and inclusive culture. Note from the Hiring ManagerWill provide relocation assistance for the right candidate.Will sponsor an existing H1B. Position Summary Seeking a Senior IT Auditor to be responsible for conducting....


Our mid-sized client is looking to add a Principal and Sr. Compliance Specialist to add to their growing team. The main responsibilities will be Field Corrective Action (FCA) and Recall Management for Medical Devices. Will be leading teams to develop field corrective action and recall plans. Oversee execution and reconciliation of field corrective actions and recalls. Working with cross-functional partners to determine root cause and population bounding as well as with Health Hazard....


T. Burks & Associates is currently recruiting for a global client who has a need for a production supervisor. This is a HIGH GROWTH position that will responsible for providing leadership to the production staff which includes coaching, personal and professional development and creating a highly effective team environment. This position is responsible for developing production area standards and goals while ensuring compliance with the Business Unit policies and procedures.....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Sales Representative for its industry leading analytical instrumentation used in R&D laboratories. This position will be covering Illinois, Wisconsin and Indiana from the Chicago area. Responsibilities:The Technical Sales Representative will be responsible for direct sales of analytical instrumentation products and services to customers in various industries like academia, food, beverage,....

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