Manufacturing Operator

We are seeking Manufacturing Operators for an exciting 6-month fixed-term contra...

Location

New Zealand , Auckland

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Proven experience in production or manufacturing within a GMP environment, with a strong emphasis on quality and adherence to SOPs
Solid understanding of Health & Safety practices and a demonstrated commitment to maintaining a safe workplace
Minimum of 3 years of manufacturing experience in pharmaceutical, animal health, food, or a related industry
Excellent written and verbal communication skills to collaborate effectively within teams
A natural mechanical aptitude and problem-solving mindset
Physical fitness is beneficial for this role, including the ability to safely handle items weighing up to 25kg as part of daily operations
Must have the right to work in New Zealand

Job Responsibility

Be competent in manufacturing and packaging operations for Solid Dose and Liquids, including operating assembly, packing and labelling equipment and performing in-process quality checks
Troubleshooting mechanical problems and providing feedback to Engineers
Maintaining a high level of housekeeping and cleanliness within the production area
Ensuring all equipment used is cleaned, calibrated and lubricated between batches
Production batch documentation is completed accurately and in compliance to cGMP standards
Compliance to Health & Safety at all times

What we offer

Competitive hourly rate and generous allowances
Comprehensive insurance cover
Access to EAP support
Fresh fruit every week
Regular on-site events

Fulltime

MS&T Scientist

The MS&T Scientist provides subject matter expertise for leading and managing ac...

Location

United States , Shawnee

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Bachelor's degree in Industrial Pharmacy, Pharmaceutics, Chemical Engineering or related scientific field
4+ years of industry experience in technology/product transfers and process optimization in a GMP environment or 2 years of industry experience with a Masters
Familiarity with processing equipment and technologies utilized in pharmaceutical GMP manufacturing facilities for solid dose, soft chewable tablets, non-sterile liquids and injectable platforms (at least in 2 areas) and sufficient experience in a commercial GMP environment
Experience in product/technology transfer activities and ability to author technical documents in support of all activities
Strong communication skills and computer literacy
Must be able to effectively interact with senior executives, senior technical managers, and external customers

Job Responsibility

Support/Lead product/technology transfers, process development, product maintenance activities establishing and optimizing commercial manufacturing processes for compounding and filling of solids, soft chewable tablets, non-sterile liquids and sterile injectable (aseptic manufacturing) platforms working closely with Manufacturing, Engineering, and Quality organizations
Generate technical protocols, reports, manufacturing documents and author Quality risk assessments to detect quality and technological risks
Lead development/engineering studies and batches
Manage and control the development of each project's work scope and schedules required for the support of key product integrations, ensuring they are completed on budget, on schedule, and technically correct
Identify critical quality attributes and the strategy for defining acceptable ranges for process parameters
Serve as single point of contact for internal teams and external customers as transfer lead for all technology and product transfers
Lead assessments regarding timelines, technical viability, resources, financial, investments, and communications needed to support product transfer activities
Support MFG efficiency and operations projects by interfacing with all internal departments (Quality, Engineering, Validation, Manufacturing, Planning, Supply Chain)
Ability to analyze and troubleshoot problems to effectively direct the activities of a cross-functional project team

Fulltime

Packaging Technology Specialist

We manufacture and supply reliable, high‑quality medicines to meet patients’ nee...

Location

United States , Durham, North Carolina; Rockville, Maryland; Waltham, Massachusetts; Philadelphia, Pennsylvania

Salary:

111375.00 - 185625.00 USD / Year

GSK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in
5+ years of experience in pharmaceutical packaging development, packaging equipment or packaging operations across multiple dose forms (e.g., solid orals, liquids, dermal, parenteral)

Job Responsibility

Lead development and introduction of first‑intent primary packaging for NPIs in the Medicines portfolio at External Manufacturing Sites
Provide packaging technology support to ensure NPI project milestones and launch dates are met
Define and deliver primary, secondary, tertiary and distribution pack designs: agree pack design briefs, evaluate design options, and ensure suitability for commercial, regulatory and manufacturing requirements
Collaborate with suppliers on component design, material selection, printing/conversion methods, cost and sustainability opportunities
Define and manage packaging functional testing (component interaction, child resistance, distribution performance, metrology) and technical review of test data and specifications
Support Packaging Validation and Production groups on equipment selection, machine trials, process qualification and control strategies to ensure robust, consistent processes
Assess and qualify packaging components, suppliers and supplier change proposals
partner with Procurement and Supplier Quality on supplier evaluations and lifecycle changes
Manage bulk packaging shipping lane qualifications and assessments for NPIs and project transfers
Identify and drive packaging improvements to reduce complexity, cost and waste while maintaining quality and compliance

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Eligibility to participate in our share based long term incentive program
Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays

Fulltime

MSAT Associate Director

Proclinical is seeking an MSAT Associate Director to oversee the successful tran...

Location

United Kingdom , Surrey

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, or Chemistry
Proven experience in site-to-site technical transfers and pharmaceutical manufacturing processes
Familiarity with small molecule formats, including sterile products, capsules, creams, gels, ointments, and solid dose
Knowledge of Quality Management Systems, including change control and deviation management
Experience in operational budget management and strategic alignment
Proficiency in project management tools, templates, and methodologies
Strong problem-solving skills and ability to adapt to high-speed changes
Excellent organizational, communication, and time management skills
Demonstrated leadership and collaboration abilities across global teams
Commitment to continuous improvement and ethical standards

Job Responsibility

Ensure adherence to GxP regulations and standard operating procedures
Lead technical transfers of manufacturing processes, providing critical expertise and direction
Establish and track KPIs, budgets, and timelines for process transfers and improvements
Represent technical expertise in cross-functional projects, including supply chain, regulatory, and commercial activities
Provide scientific advice to procurement and regulatory teams, addressing batch failures, recalls, and variations
Conduct technical reviews and due diligence for potential acquisitions and divestments
Collaborate with manufacturing sites to optimize processes and resolve compliance or quality issues
Review and approve technical documentation, including certificates of analysis, stability data, and risk assessments
Manage quality records such as change control requests and deviations
Propose and implement technical and business improvements to enhance practices and systems

Fulltime

Sr. Team Leader - Equipment Maintenance

The Engineering Shift Lead for the IMA Filling Line is responsible for leading t...

Location

India , Vizag

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Diploma (or equivalent) with 10+ years of experience or associate’s degree with 8+ years of experience or BA/BS with 5+ years of experience or MBA/MS with any years of relevant experience
Strong expertise in equipment and project management
Demonstrated direct supervisory experience
Solid understanding of knowledge management
Proficiency in Good Manufacturing Practices (including cGMP), OSHA, FDA, and environmental regulations relevant to the pharmaceutical industry
Strong English speaking and writing abilities

Job Responsibility

Lead mechanical/Instrumentation troubleshooting of IMA filling line equipment (e.g., sensors, PLC, conveyors, dosing units, sealing systems, servo mechanisms)
Ensure minimum downtime by providing quick and effective diagnostic responses to mechanical failures
Guide team members on root cause analysis, FMEA and corrective actions
Oversee execution of shift-level preventive maintenance (PM) activities as per schedule
Ensure proper lubrication, alignment, precision adjustments, and mechanical integrity checks
Identify recurring issues and propose reliability improvements
Lead and supervise a team of Team members and operators during the shift
Coordinate with Manufacturing, quality, safety, and warehouse teams to ensure smooth operations
Conduct shift handover meetings with accurate reporting of issues, breakdowns, and follow-up actions
Drive improvements in line efficiency (OEE), waste reduction, and equipment performance

Fulltime

Senior Process Engineer

Location

Canada , Mississauga

Salary:

Not provided

Advanced Technology Search Group

Expiration Date

Until further notice

Requirements

Minimum 10 years’ experience in leading the design/construction of capital and CI projects in a fast paced, high-technology, team environment, preferably in the pharmaceutical or food industry, with at least of 3 years in leadership experience
In depth technical understanding of relevant unit operations in the pharmaceutical industry, their capabilities and associated processes. High preference for liquid and semi-solid dose operations
Proven track record in managing major capital and CI projects in a team environment “on time and on budget”
In depth understanding of automated / integrated production equipment and computerized systems
In depth knowledge in the qualification and validation of equipment, facility and processes. Proficiency in the creation of qualification documentation with minimal supervision
Experience in managing customers, vendors, consultants and contractors
Proven leadership capabilities/competencies, and ability to manage teams and reach objectives without formal reporting relationships
Knowledgeable in the numerous regulatory aspects of capital construction, including the Occupational Health and Safety Act, the Ontario Building Code, the Boiler and Pressure Vessel Act, etc.
PEO (Professional Engineer of Ontario) designation eligibility - P. Eng. preferred

Job Responsibility

Working with members of the Engineering Team, assemble the appropriate project team to execute each project through concept development, scope definition and estimating, design, and construction execution. An important part of this role is the understanding of the end user requirements through ongoing consultation with representatives of those customer groups
Use mechanical, electrical and/or process systems expertise to work with individual Project Delivery Teams to ensure the appropriate commissioning, qualification and training plans with accompanying resources are in place to deliver efficient system start-up
In cooperation with other project leadership team members, ensure that all systems are in place to ensure due diligence in design and construction procurement/execution and project cost and schedule controls
Ensure that all work is performed in full compliance with established regulatory standards including, but not limited to, company safety policies and procedures, cGMP, building code and MOL/MOE requirements
Lead the development and ongoing maintenance of engineering design and construction standards and ensure compliance on all project executions
Support as required the trouble-shooting and problem resolution of facility systems and operational equipment
Ensure all necessary permits, as required by the current codes, are obtained and that any necessary inspections are scheduled
Lead and support the development and execution of F.A.T-, commissioning and validation requirements and associated documentation for work assigned, as required
Actively supports the Business Development (BD) team in the introduction of new products and modifications of existing products. Provide technical support to BD on creation of new routing and provide process flows for the manufacturing and packaging of new products and/or modification of existing products
Leads customer process optimization and investigations, equipment selection and customer audits and visits

Fulltime

New

IT Training Lead

The IT Training Lead will drive technology learning and user adoption across the...

Location

United States , Delray Beach

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Experience in IT training, instructional design, technical enablement, or learning and development
Strong knowledge of Microsoft 365
Excellent communication, facilitation, and content development skills
Ability to translate technical concepts into practical, user-friendly training.

Job Responsibility

Design, develop, and deliver IT training programs in instructor-led, virtual, and self-paced formats
Take lead in the Microsoft Copilot and AI training strategy, including onboarding, advanced use cases, responsible AI usage, and ongoing enablement
Partner with IT leadership to support new technology rollouts, system upgrades, and digital transformation initiatives
Create and maintain training content, including videos, guides, tutorials, and job aids
Identify skill gaps and develop targeted learning solutions to improve adoption and productivity
Gather feedback and measure training effectiveness to continuously improve programs.

New

K Kitchen Representative

The position includes, but is not limited to, the following essential job duties...

Location

United States , New Albany

Salary:

Not provided

Circle K

Expiration Date

Until further notice

Requirements

Excellent communication skills
Team player who can work well with others or independently
Acts with integrity
keeps commitments
Contagious positive attitude
Focuses on achieving results while having fun
Frequently bend, twist at waist, kneel, squat, stand, and walk
Occasionally climb and descend ladders
Tolerate extreme cold and hot temperatures and work in and around fryers, ovens, grills, coolers, freezers, sharp objects, and loud noises
Reach, grasp, and manipulate objects with hands for entire shift, including reaching for objects overhead

Job Responsibility

Provides excellent guest service in a fast and friendly manner
Maintains a clean restaurant environment by cleaning and performing general housekeeping duties
Prepares and serves food items in accordance with all Brand, Company, and health department regulations
Ensures product quality, food safety, and operational standards are met
Keeps accurate cash, sales, and inventory control records
Follows all government laws and safety codes
Completes reports on all incidents following our 5-minute rule policy
Lives our Company values: One Team, Do the Right Thing, Takes Ownership, Play to Win

What we offer

Medical, Dental, Vision, Term Life and AD&D plans
Flexible spending and health savings accounts (FT)
Vacation paid time off
Company holidays paid at time and a half
Matching 401(k)
Tuition Reimbursement
Stock Purchase Plan
Employee Discount Program
Discount Meal Benefit
Wellness Plan

Select Country

Manufacturing Operator - Solid Dose

Job Description

Job Responsibility

Requirements

What we offer

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