UNKNOWN

FEED

Perform the daily setup and routine operation of the packaging line, including but not limited to: bottle in-feed, unscrambler, filler, bottle capper, torquer, labeler, vision systems, weighing systems, bar coding systems, sealers, disassembly/assembly, cleaning, resolving equipment stoppages and jams, and all material handling as trained. Complete, maintain, and update production documentation (both electronic and paper) to perform material movements, material take-outs and yield determinations by following SOPs and utilizing systems as required such as Systems/Applications/Products (SAP), Manufacturing Execution Systems (MES), Electronic Batch Records (EBRs), etc.

Argenta Global

Manufacturing Operator - 3Rd Shift Liquids Compounding (Sunday - Thursday 10:00 PM - 06:30 AM

ea_via_bold

Rights Compliance CoordinatorSean McGeeney, SuperintendentPO BOX 157; White Salmon WA 98672Telephone Number: 509-493-1500Email: sean.mcgeeney@whitesalmonschools.org. In all personal contact with the student athlete, officials, Athletic/Activity directors, school administrators, the WIAA, the media and the public, the coach shall strive to set an example of the highest ethical and moral conduct.

White Salmon Valley School District

Head Girls' Basketball Coach-HMS

linkup_via_bold

Key Responsibilities: Manage, lead and oversee all aspects of Quality department across Americas CRO embedding quality within operations and facilities using a risk-based, science-based approach Develop and implement quality strategies that ensure scientific integrity, regulatory compliance, operational excellence and continuous improvement leading to controlled documentation and sustained inspection/audit readiness Oversee QA and QC functions across business units within Americas CRO ensuring consistency and compliance Build and lead a high performing team, embedding a culture of quality through coaching, training and cross-functional partnership Manage and maintain quality systems and files across Americas CRO Coordinate and perform internal audits and activities as requested Perform qualification inspections/audits of selected vendors, laboratories, and clinical study sites Conduct inspections/audits of company SOP programs and files (Qualification and Training files, SOP systems, Archiving, etc.) Perform follow-up reviews of audit findings to confirm corrective actions have been completed Provide oversight and participation in inspections by regulatory agencies and clients Ensure the team has the skillset to support the following: drafting of QA and Data Management Plans, full capability to ensure drugs received for studies comply with regulatory, protocol and SOP compliance, auditing of protocols and Final Study Reports. About You: Bachelor's degree, preferably in a scientific discipline or equivalent experience Minimum of 10 years' experience in a quality role in a highly regulated industry, including 4+ years of supervisory experience Animal Health experience highly preferred Demonstrated autonomy to lead a large, multi-functional quality department, drive enterprise-wide quality strategy, and partner with executive and operational stakeholders in a regulated environment Progressive quality leadership experience in GCP and GLP compliant organizations A collaborative working style to be able to lead and motivate people at all levels and across all functions in an organization Experience conducting/acting as lead auditor for external audits Experience conducting audits of study protocols in accordance with GCP guidance Experience conducting study data audits Experience auditing study reports (Final Study Reports (FSRs) Experience conducting internal inspections/audits.

Argenta Ltd

Director of Quality

If you have a steadfast drive, validated leadership skills, and a quantitative mentality ready for a new challenge to accelerate your personal growth, Chewy may be the right environment to improve your career success while boldly innovating how we “wow” our customers and team members. •* Manage the inbound, outbound, and inventory control activities within one of our Fulfillment Centers (FC) to ensure timely picking, packing, and shipping of customer orders while maintaining on-time shipments and minimal shipment defects.

<p>Amazon changed how we shop for books. Netflix transformed the way we consume movies. At online pet specialty retailer Chewy, we’re disrupting the pet products industry by offering our customers the easiest way to get the premium products they want, backed by unparalleled service. We strive to win at everything we do, whether that means bending over backwards to gain our customers’ trust and loyalty or creating a creative and stimulating work environment for our employees. We aim to wow our customers—and our employees. Trust us. You’ll notice the difference from the moment you become a candidate with us.

At Chewy, we believe in ownership and accountability and value creativity. We are makers and doers who thrive on the desire to drive results. We approach our mission to provide the best service and pet products anywhere with a dogged determination and a disposition that’s as sunny as the South Florida oceanfront we call home. Sure, we work hard, but we have fun, too. Of course, that’s not hard to do when you get to bring your favorite four-legged friend to the office. </p>

Chewy

Transitioning Military Service Member, Area Manager

Essential Job Functions: The incumbent must be able to perform all the following duties and responsibilities with or without reasonable accommodation: Greet clients and patients arriving for appointments or walk-ins and escort into an exam room, obtain weight and vital signs (temperature, pulse, respirations, pain score, body condition score), record all in the electronic medical record, and begin documentation of the patient visit in the electronic medical record by obtaining and recording a thorough patient history. Prepare patients for surgical and dental procedures, safely support induction and monitoring of anesthetized patients including checking and recording vital parameters (under direction of the veterinarian), monitor patients during recovery, and prepare them for discharge to owner or transfer to an overnight care facility as needed.

Petco Animal Supplies Inc

Registered Veterinary Technician

A well-established small animal practice in Missouri City, Texas is seeking an Associate Veterinarian to join its experienced and supportive medical team. For more information, please contact: Sam Ortiz Senior Talent Acquisition Specialist (954) 323-4373 Careers@desortstaffing.com .

Desort

Associate Veterinarian – Balanced Professional Schedule

Lead the activities to develop microbiological methods to assess the purity, potency, other key attributes, and stability of drug substances and finished products performing testing including sterility, endotoxin, bioburden/microbial limits, ELISA, sub visible particulate, and microbial identifications. Key Responsibilities: Performs and maintains accurate, detailed records for method development/optimization, method transfer/suitability/validation, and for routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications to pharmaceutical cGMP requirements.

Microbiologist, Msat

Key Responsibilities: Performs and maintains accurate, detailed records for method development/optimization, method transfer/verification/validation, and for routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications to pharmaceutical cGMP requirements. About You: Bachelor's degree in chemistry or related Science field with work experience in cGMP and/or GLP chemistry lab environment (a minimum of 2 years of work experience with B.S. or 1 year of work experience with masters (M.S) is preferred.).

Chemist, Msat

Key Responsibilities: Performs and maintains accurate, detailed records for method development/optimization, method transfer/verification/validation, and for routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications to pharmaceutical cGMP requirements. About You: Bachelor's degree in chemistry or related Science field with work experience in cGMP and/or GLP chemistry lab environment (a minimum of 6 years of work experience with B.S. or 3 years of work experience with masters (M.S) is preferred.).

Senior Chemist, Msat

This role serves as the coordination hub between customers and internal technical teams, ensuring programs progress efficiently, compliantly, and in alignment with business commitments. Provide regular portfolio-level reporting to PMO leadership and senior stakeholders, with clear visibility of progress, risks, and decision points across all active programs.

Tech Transfer Project Manager

Support/Lead product/technology transfers, process development, product maintenance activities establishing and optimizing commercial manufacturing processes for compounding and filling of solids working closely with Manufacturing, Engineering, and Quality organizations. leading and managing activities including product/technology transfers, innovation, and process optimization for pharmaceutical products for Oral Solid Dose, Soft Chewable Tablets, Non- sterile liquids or Injectable technology platforms.

Manufacturing Science & Technology (Ms&T) Scientist

Will work closely with Product Supply personnel within Engineering, Maintenance, Production, Quality & Technical Service Groups to understand current production processes/issues, initiate and support process improvements and improve maintenance procedures in support of system reliability. Actively participates during all phases of equipment life cycle by supporting the development of specifications, design and installation of equipment, systems, facilities, and utilities, and processes to ensure compliance to cGMP requirements.

Senior Plant Engineer

The Plant Automation Engineer also designs and implements new technologies, system upgrades, and replacements, while developing and maintaining software code, HMI graphics, databases, and system configurations to ensure safe, compliant, and efficient operations. This role provides technical leadership and project management support for utility, process, and facility automation systems and serves as the site Subject Matter Expert (SME) for controls and automation.

Plant Automation Engineer

Duties: Develop User Requirement Specifications (URS), Functional Requirements (FRS), Configuration/Design Specifications, Risk Assessments, Requirement Traceability Matrices (RTMs), Validation Plans (VMP), Test Plans, and Validation Summary Reports (VSR). Requirements: Bachelor's degree in Engineering, Life Sciences, Pharmaceutical Sciences, or a closely related field, and 2 years of experience in pharmaceutical validation, quality systems, or related GMP-regulated environments.

Validation Specialist

Performs and maintains accurate, detailed records for method development/optimization, method transfer/verification/validation, and for routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications to pharmaceutical cGMP requirements. About You: Bachelor's degree in chemistry or related Science field with work experience in cGMP and/or GLP chemistry lab environment (a minimum of 8+ years of work experience with B.S. or 6+ years of work experience with masters (M.S) is preferred).

Senior Scientist, Science & Technology

Identify and pursue new regulatory consulting opportunities which may include meeting with new clients, traveling and speaking at professional meetings, networking in the industry and contributing to various publications. We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role.

Senior Regulatory Affairs Manager

The caseload includes dogs, cats, and a full range of exotics such as rabbits, ferrets, guinea pigs, pocket pets, and reptiles, along with GP and urgent care cases. $120,000 to $140,000 annual base salary, plus production bonus (ProSal) with no negative accrual.

Redbirdjobs

Associate Veterinarian, Exotics & GP, 3- or 4-Day Week

Manatal

Microbiologist, MSAT

Conduct qualitative and quantitative chemical analysis and experiments for active pharmaceutical ingredients and pharmaceutical products as per project requirements Assist in the development of new products and processes as per compliance and regulatory requirements Assist with the technology transfer (methods and products) from Argenta Research into Argenta Manufacturing Support the Research & Development efforts of the company by providing scientific and technical support for the development of new products. Create and maintain activity plans for assigned projects Generate, document and review technical data for internal reports, client reports and CMC regulatory support documents.

R&D Analytical Scientist

Key Responsibilities: Performs and maintains accurate, detailed records for method development/optimization, method transfer/verification/validation, and for routine analysis of finished pharmaceutical dosages and/or raw materials following approved analytical methodology and specifications to pharmaceutical cGMP requirements. Knowledge of GMP and FDA manufacturing regulations Ability to analyze and interpret data Strong written and oral communication skills Demonstrated knowledge & awareness of current industry issues & evolving trends in the regulated environment; both domestically & internationally.

Animal Care Jobs in Blue Springs, MO

Manufacturing Operator - 3Rd Shift Liquids Compounding (Sunday - Thursday 10:00 PM - 06:30 AM Argenta Global

Head Girls' Basketball Coach-HMS White Salmon Valley School District

Director of Quality Argenta Ltd

Transitioning Military Service Member, Area Manager Chewy

Registered Veterinary Technician Petco Animal Supplies Inc

Associate Veterinarian – Balanced Professional Schedule Desort

Microbiologist, Msat Argenta Global

Chemist, Msat Argenta Global

Senior Chemist, Msat Argenta Global

Tech Transfer Project Manager Argenta Global

Manufacturing Science & Technology (Ms&T) Scientist Argenta Global

Senior Plant Engineer Argenta Global

Plant Automation Engineer Argenta Global

Validation Specialist Argenta Global

Senior Scientist, Science & Technology Argenta Global

Senior Regulatory Affairs Manager Argenta Global

Associate Veterinarian, Exotics & GP, 3- or 4-Day Week Redbirdjobs

Microbiologist, MSAT Argenta Ltd

R&D Analytical Scientist Argenta Ltd

Senior Chemist, MSAT Argenta Ltd

Similar Job Searches

See More Jobs

Get noticed by top employers!