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- Any US State
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Title: Quality Assurance QA Release and Inspection Inspect pharmaceutical finished product received at warehouse facility. Perform finished product release activities to established procedures ensuring appropriate material labeling. QualificationsEducation: BS Biology, Chemistry, Engineering or equivalent experience within a pharmaceutical setting (required)

- Santa Cruz, CA
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Manufacturer of confection based dietary supplements and nutritional vitamins supplying the sports nutrition, natural product and nutraceutical markets. 200K sq.ft. Plant with 500 employees, 5-day, 3 shift, 3 mogul lines, 14 packaging lines, producing 30mm products daily. Company holds 37% of this market. Responsibilities: Hands-on position that oversees and manages the day-to-day facility operations and maintenance of buildings, environmental compliance and safety program. Support the....

- Santa Cruz, CA
new job!

Manufacturer of confection based dietary supplements and nutritional vitamins supplying the sports nutrition, natural product and nutraceutical markets. 200K sq.ft. Plant with 500 employees, 5-day, 3 shift, 3 mogul lines, 14 packaging lines, producing 30mm products daily. Company holds 37% of this market. Responsibilities: Prevention of serious incidents through high risk activity management processes, emergency response planning, safety in operations and contractor safety. Responsible for....

- Marshfield, MO
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(Shift position) Supervise departmental operations of the packaging department Provide leadership to all department personnel Schedule production personnel to meet customer requirements Maintain compliance with quality assurance, governmental and auditing agencies Assist department in solving problems such as production scheduling and packaging problems Deal with employee problems and complaints. Ensure standards are kept safety, maintenance and preventive maintenance matters. Take necessary....

- Algonquin, MD
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Job Description: Supervise mechanics and maintenance staff in accordance with all policies implemented by the companyPerforms Maintenance, Repair and Preventative Maintenance of Aseptic packaging lines.Maintain the operation of the production equipment by working with operators and other staff to identify and correct potential issues that could create downtime.Assisting other departments where needed as directed by managementWorking closely with the Maintenance Manager, Maintenance....

- San Francisco, CA
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DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....


Unique Opportunity!This position intersects Coatings / Formulations / Process Engineering / New Application Development / Manufacturing.Looking for a SME Principal Engineer in Oral Solid Dose, preferably an Organic Chemist that has moved from the bench to a coatings manufacturing environment but still involved in formulations, troubleshooting. Company offers cutting edge technology, a leadership role, an opportunity to interface with executive management and provide manufacturing solutions to....

- San Francisco, CA
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Our client in the San Francisco Bay area, has a new opportunity for Medical Director with expertise in Oncology NGS. This is a full-time, onsite position, with the opportunity to make an impact, company is seeking a driver to lead change. Medical Director, Oncology NGS San Francisco Bay AreaServes as company’s internal and external oncology / medical expert collaborating with several departments / business units including marketing, market access, salesRespond to questions from physicians and....

- San Francisco, CA
new job!

Vice President, Regulatory Affairs San Francisco Bay Area Our client is seeking a Vice President, Regulatory Affairs who will be responsible for regulatory strategy, oversight, and guidance drug development program. The successful candidate will bring strong leadership abilities to oversee the Regulatory Affairs team, a successful history of effectively leading IND and NDA filings through approval, and interacting effectively with the FDA and other foreign regulatory bodies. This position....

- San Francisco Bay Area, CA
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DIRECTOR, REGULATORY AFFAIRS – CMCSan Francisco Bay Area Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout....

- Garden City, KS
new job!

TITLE: PHARMACIST LOCATION: Western Kansas Are you interested in making a difference in patient care? Are you looking for a facility that is interested in candidates that want to grow professionally but have not been given the opportunity? Would you like to work in a facility that serves several counties and can offer small town living with lots of outdoor activities and within a few hours of some larger cities? Then this could be an opportunity for you. Here is some details: An unique....

- Wyckoff, NJ
new job!

My client offers an outstanding culture and exceptional benefits, and they seek a meticulous Technical Writer to oversee a small group and take on the following tasks:Direct the overall process for creating, editing and publishing client reportsOversee variable workload by assigning and coordinating the work of othersEnsure the timely preparation of all manuscripts and responses to reviewer commentsServe as the internal editor-in-chief to establish and maintain a high-quality written....

- Madison, WI
new job!

We are working with a client in the Madison area in need of a Senior Quality Control Analyst. This client is a manufacturer of pharmaceutical ingredients. This position is for an experienced analyst with experience in qPCR and molecular technologies. This opportunity requires this person to be independent and a creative thinker. Responsibilities:Responsible for performing complex and routine laboratory analysis and testing of raw material, finished product and special products.All work is....

- Springfield, MO
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PRODUCTION SUPERVISOR This position is responsible for the supervision and oversight of daily activities in the Packaging Department of the plant. Will supervise 25+ union employees on the night shift (5pm - 5am). Shift is constant but days rotate - so every other week you have a 3-day weekend (3-2-2-3). Requirements:Willing to work 5pm-5am on a rotating day basis (3-2-2-3) is a requirement.BS Degree is Required.2+ years minimum experience as a Production or Packaging Supervisor in....

- close to Deming, NM
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TITLE: Clinical Staff Pharmacist LOCATION: close to Deming, NM Would you like live and work in an area that can offer a little bit of everything? Would you like to live in an area that has sunshine almost every day of the year? How about finding a career and life balance? Where could you go and have a positive affect on patient care and enjoy breathtaking sunsets on the mountains, river activities and a mixture of outdoors as well as bountiful indoor activities for anyone of any age? The....

- St. Louis, MO
new job!

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

- Cambridge, MA
new job!

My client seeks an outstanding scientist to contribute to drug discovery and development projects. The ideal candidate will work closely with medicinal chemists and other scientists – and apply methods to improve drug properties and efficacy. In addition, this person will apply and develop cutting-edge techniques and interpret data using modeling and data mining. Finally, the ideal candidate will possess leadership qualities to direct projects and collaborations. The level of the position is....


Report and Database ManagementServe as administrator for Focus (external database); identify and resolve sales related errors or discrepancies on an as needed basis; manages filters to separate sales data by veterinary and OTC division and exclude any diversion or ALT/ALC (online) accounts.Update territories and view capabilities; maintain Focus item master.Create templates and generate reports in Focus and ProDecisions (internal database) for product managers, sales team, and management on an

- outside of Wichita, KS

TITLE: Medical Technologist LOCATION: Outside of Wichita, Kansas Are you looking for a new position where you can live and work in a community that offers big city conveniences in a micropolitan atmosphere so you can have the best of both worlds. Would you be interested in working for a healthcare leader in the region? Would you like to live in an area that is affordable and has low crime? Do you like to have a work life balance and live in an area with beautiful scenery and friendly people....


Primary Care facility providing services for a large pediatric population is expanding and needs to add a Nurse Practitioner for Pediatrics. * COMPENSATION is 80k to 83k. * JOB TYPE is Permanent/Retained Employee, Full-time. * WORK SCHEDULE is Monday through Friday, approximately 8am to 4:00 pm, which totals approximately a 36 hour work week. * LICENSE and EDUCATION required for a Nurse Practitioner is a application for or possession of a New York State license, DEA#, CPR, PALS, and ACLS. NEW....

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