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- Lancaster, SC
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The Manufacturing Operator reports to Manufacturing/Packaging Supervisor and is responsible to follow written and/or verbal instruction issued by the Supervisor or Team Leader/designee, to set-up plant equipment correctly for operation, organize work to achieve daily production schedules with no errors or deficiencies, follow and adhere to all Standard Operating Procedures, Safety Policies, Company Policies and Procedures, cGMP guidelines and effectively use time to meet company goals and....

- Lancaster, SC
new job!

Maintenance Mechanic POSITION SUMMARY Preventive and breakdown maintenance on packaging equipment. Inspect, test, adjust, maintain, and repair all electronic, mechanical, and electrical equipment. Test equipment and instruments, wiring diagrams and drawings, blue prints and sketches, and electrical tools. Calibrate and test equipment, assorted hand tools, power tools, and all shop equipment. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned as....

- Lancaster, SC
new job!

The Customer Service Representative is responsible for providing incoming/outbound call center support for consumer and veterinary customers.Roles and Responsibilities:Answer inbound calls.Categorize all incoming calls.Escalate calls as necessary to Team Leader, Technical Services or Manager.Process customer orders.Setting-up new accounts in FACTS (obtain required license vet professional or consumer professional.)Processing literature requests using the Literature Database.Run weekly Order....

- Lancaster, SC
new job!

The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices.The QCC will assist in evaluating new testing applications and instrumentation, either developing methods or adopting compendial methods. This person will aid in....

- Winston-Salem, NC
new job!

Join a global leader as a Eco-Toxicologist responsible for conducting quantitative environmental risk assessments for agrichemical and fertilizer products and traits in North America. You will provide technical advice on study designs for regulatory and research oriented studies as well as advice to support new and existing registrations of client products and traits. --- Work closely with regional/global regulatory and product safety teams as well as other functional teams to produce risk....

- Any US State
new job!

Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....

- Pleasanton, CA
new job!

Our large drug/device combo client in Irvine, CA needs a temporary Regulatory Affairs Associate. This contract is estimated to last 12 weeks. This person will coordinate most aspects of company regulatory activities and may interface with domestic and international health authorities. Qualifications: - BS or BA degree, 1-3 years of experience in regulatory affairs. - Experience in a company start-up environment, preferably in medical devices or combination products. - Knowledge of FDA, CA-FDB,

- Los Angeles, CA
new job!

Grow your career while working and being trained in the exciting field of Oncology Clinical Research. This opportunity is for a large growing clinical trial site in W. Los Angeles. Requirements:*Experienced Oncology Nurse (RN required, OCN is a plus) *CA License*Must be able to follow the protocol and see that it is followed*Good communication skills and work well with patients and doctors *Full-time Mon-Fri *Must be commutable to W. Los Angeles Responsibilities may include: - Screening....


Our client, a small start-up company who was recently recognized as an award-winning Top Workplace is looking to add to their growing team. The Principal Regulatory Specialist will be working on a variety of worldwide pre-market and post-market regulatory activities. The first project will be working on the early (concept) stage of a submission. Responsibilities: - Support the Senior Manager of Regulatory in developing a partnership with other departments in designing and enhancing regulatory....

- Seattle OR San Fran, Cali, WA
new job!

Top tier Pharmaceutical company in Seattle, WA is expanding They are opening new office as well i nthe San Francisco Bay area of Califronia- this role can be located in either location Full benefits-medical/health, 401k and match, stock, LTis and STis...many progressive benefits...competitive compensation and bonus and more... Full relocation to either area The Sr. Director, Clinical Operations Program Management will be responsible for leading all aspects of clinical operations within the....


Traditional SHE leader's role dealing with a Chemical manufacturing facility. MUST HAVE PSM BACKGROUND AND EXPERIENCE. Will not even look at anyone without it. Lead the plant’s safety, health, environmental and security programs, as well as the operation of the Utilities function. Take the lead on all compliance with all safety and environmental regulations and policies. Lead effort in compliance with environmental regulations, permits and reporting requirements. Responsible for the operation....


RETAINED SEARCH ASSIGNMENT Quality Assurance Validation, ManagerVMP – Validation to include: Facility, Utilities, Equipment, Computer, etc.QA Validation MgrMUST have Bio Pharma experienceManage Validation, Write Protocols,Manage EquipmentProject Manager for all Validation ProjectsResponsible that Validations are prepared and executedDesign Validation studies; USA & EUExecute CAPA action plan9CFRDegree BS a Science or relatedPrefer 2+ yrs supervision & experience designing and....

- Any US State

Validation Manager To manage all validation activities at the plant. This includes but is not limited to facility, equipment, cleaning, computer and process validation. This position will lead the site to ensure compliance to all applicable regulations and requirements. Ensures implementation of compliant validation master plan for the site and ensures all activities within the master plan are planned and executed. Writes, reviews and executes any required validation protocols to ensure....


This world class chemical client is seeking postdoctoral scientists to develop new models and algorithms in the area of Supply Chain and Production optimization, transportation, planning and logistics to improve the sustainability of products and our business in line with the Growth Plan. In this position, you will have the opportunity to help shape how the clients approaches complex problems such as demand forecasting, product placement and supply optimization. Responsibilities: --- Create....


Relocation assistance to Tulsa, OK approved for this position. Key requirements for candidates: - Experience in New Product Development quality aspects for medical devices - Able to deal at high level across technologies that might be out of his core competencies - Awareness of international medical standards and regulations - Risk management for medical device (14971) - Ability to work in great autonomy since remote from the rest of the team - Engaging and communicating effectively. Other....


Lead the development and execution of all engineering and construction projects associated with midstream natural gas production, compression, and transmission for energy clients throughout the Marcellus and Utica Shale plays. As the principal Mechanical Lead and Subject Matter Expert (SME) for all midstream and upstream operations, you will support new business development in securing EPC work with a variety energy companies throughout the western PA, eastern OH, and WV. The Mechanical Lead....


Lead the development and execution of all engineering and construction projects associated with midstream natural gas production, compression, and transmission for energy clients throughout the Marcellus and Utica Shale plays. As the principal Mechanical Lead and Subject Matter Expert (SME) for all midstream and upstream operations, you will support new business development in securing EPC work with a variety energy companies throughout the western PA, eastern OH, and WV. The Mechanical Lead....


Title: Pharmaceutical CMC Manager Oversees research efforts of the CMC team within the Pharmaceutical Development Group. Evaluates needed resources to meet the project expectations for CMC support and anticipates gaps to avoid project delays. Formulates a plan for building the CMC section of each project. Coordinates with key players inside and outside Research & Development to ensure CMC needs are met BS in Chemistry, Engineering, or related science10 years experience in chemistry-related

- St. Louis, MO

Our client - a major Pharmaceutical company located in St. Louis - is looking for a Manager / Sr. Manager - QC. The Manager / Sr. Manager will be responsible for overseeing all aspects of the QC Laboratories to include raw materials, finished goods etc. They will also manage the review and approval of specifications and test methods for finished goods and raw material methods. Additionally, they will ensure that resources are utilized to ensure timely turnaround time for finished goods and raw

- Boston, MA

Highly successful technology company seeks a skilled Applied Scientist to join their specialized Search engineering team. This team helps build and power the engine that responds to tens of billions of queries per day, searching through terabytes of data in milliseconds. This team designs, builds, and deploys high performance, fault-tolerant distributed search systems used by millions of people every day.The search team is also responsible for building a platform that will enhance the customer

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