Quality Associate Job at Randstad (Sydney)

Associate Quality Control

The Associate Quality Control will provide analytical testing support for the Qu...

Location

United States , Thousand Oaks

Salary:

66222.00 - 82012.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 2 years Quality Control experience
Associate’s + 6 months Quality Control work experience
Bachelor’s

Job Responsibility

Execution of QC Microbiology assays following assigned procedures
Analysis of analytical test results and reporting of raw data into various laboratory information management systems
Lab support activities such as management of lab consumables and equipment maintenance/work order completion
Operating specialized laboratory equipment
Daily communication and collaboration with cross-functional teams
Implementation of lab improvements to ensure an efficient and productive lab environment
Flexibility in work hours to support demand of work
occasional evening and/or weekend hours may be required

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans

Fulltime

Manufacturing associate

BioMarin’s Technical Operations group is responsible for creating our drugs for ...

Location

United States , Novato

Salary:

15.00 - 30.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s degree in science related area or engineering
Associate’s degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry
Strong communication skills—verbal and written
Ability to work in a team environment which includes good conflict resolution and collaboration
Displays good initiative to identify areas for improvement and implement solutions
Understanding of cGMPs as related to Commercial Operations
Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.)
Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance
Gain experience with automation systems (LIMS, MES, PI, etc.)
Ability to participate on projects and contribute to outcomes

Job Responsibility

Understanding of process theory and equipment operation
Support initiatives for process optimization
Identify and elevate processing issues and support solutions
Provide feedback and/or suggested changes to operational procedures
Assist in the incorporation of new technologies, practices, and standards into procedures
Capable of writing and reviewing process documents

What we offer

discretionary annual bonus
discretionary stock-based long-term incentives
paid time off
company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Drapery Finishing Associate

The Memory Stitch role involves hand-sewing each pleat with loop cord using a se...

Location

United States , Augusta

Salary:

13.00 USD / Hour

Hunter Douglas

Expiration Date

Until further notice

Requirements

High school graduate
Sewing experience
Able to use and read a tape measure
General knowledge of fabrics
Ability to use hand tools
Successfully pass color blind test
Accuracy with names, numbers and spelling
Capable of sitting for extended periods of time
Strong attention to details
Follow written and verbal instructions

Job Responsibility

Remove drapery from rack for processing
Assist the Pleat Folder in placing drapery neatly on the fan folding machine
Fold long draperies manually on the worktable
Hand-sew each pleat using loop cord and a sewing needle
Refold and band draperies in preparation for inspection
Send finished draperies to the inspector for final quality check
Perform other related duties as assigned by the supervisor
Comply with all facility safety rules and regulations
Report unsafe practices, conditions, or near misses immediately to a supervisor
Maintain floor safety discipline and intervene in cases of unsafe behaviors

What we offer

Generous benefits package including medical, dental, vision, life, disability
A company culture that prioritizes internal development and professional growth
Time off with pay
401(k) plan with a degree of employer matching
Paid parental leave
Wellness programs and product discounts

Fulltime

Transcription Operations Associate

As a Transcription Operations Associate in the Americas region, you will enable ...

Location

United States , New York

Salary:

75000.00 USD / Year

AlphaSights

Expiration Date

Until further notice

Requirements

Bachelor’s degree, with strong academic credentials in any field and noteworthy extracurricular leadership
No prior work experience is needed. However, relevant internships and other evidence of interest / experience working in operations in a service or business context, are desirable
Track record of strong academic performance (minimum GPA of 3.5)
Fluency in written and spoken English is essential

Job Responsibility

Production Oversight: Managing transcription orders, prioritizing unclaimed tasks, and addressing queries and capacity gaps for efficient production. You will be responsible for ensuring that we are meeting industry-leading turnaround time, quality, and cost-efficiency at scale
Issue Resolution: Independently addressing issues that affect transcription service delivery, while leveraging internal teams for troubleshooting as required
Contractor Management: Building and overseeing a skilled contractor team in your region. You will be responsible for your unit KPIs, ensuring a productive and engaged contractor community, while also collaborating with our Transcription Quality Assurance team to improve quality metrics

What we offer

17 vacation days
10 company holidays
an end of year break between Christmas Day and New Year’s Day
Competitive medical, dental, and vision insurance
401(k) match – 4% of your total compensation matched dollar-for-dollar
Prime midtown office with state-of-the-art amenities
The option to work from home on Fridays

Fulltime

Lead Packing Associate

The Lead Packer is responsible to ensure only good quality products are packaged...

Location

Canada , Brampton

Salary:

Not provided

Can Art Aluminum Extrusion

Expiration Date

Until further notice

Requirements

High school diploma or equivalent
Minimum 2 years' experience in a warehousing or packaging role
Must be able to read and write in English
Able to work at a quick pace with strong attention to detail
Excellent organizational, time management and multitasking skills
Team player that is able to work with little to no supervision
Knowledge of health and safety best practices in a manufacturing environment

Job Responsibility

Ensure that all product is packaged according to the specific packaging instructions
Inspect material for any potential defects and report any quality concerns to the packaging team leader
Ensure material is packed in order of priority according to the ship dates indicated on the work order
Ensure hardness is checked and documented per order
Confirm that weights and piece counts of each order is correct
Record product, packaging, and order information on specified forms and records
Print tickets/labels for bundles using Epics
Comply with all quality related policies, procedures, and system requirements
Use hand tools such as staple guns or nail guns for the purpose of making skids
Assist in providing training and support to new workers

What we offer

Company paid benefits (Extended Health Care, Vision Care, Dental Care, Life Insurance)
Competitive Wages
Immediate RRSP Match
Opportunity to work overtime
Paid Breaks
Training and Opportunity for advancement
Monthly employee appreciation day with lunches
BBQ/Ice Cream trucks during the summer
Employee safety shoe and prescription safety glasses reimbursement

Fulltime

Senior Associate Quality Assurance

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States , New Albany

Salary:

82081.95 - 111052.05 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 4 years quality work experience
Associate’s + 2 years quality work experience
Bachelor’s + 6 months quality work experience
Master's
Bachelor’s degree in Life Sciences, Engineering, or related field
1+ years of experience in Quality Assurance within a GMP environment (biotech/pharma preferred)
Strong knowledge of cGMP regulations and industry best practices
Experience with batch record review, and deviations
Ability to work flexible shifts, including evenings, nights, weekends, or holidays as needed
Excellent communication, problem-solving, and organizational skills

Job Responsibility

Providing on-the-floor QA support for manufacturing activities across assigned shifts
Ensuring adherence to GMP regulations and internal quality standards
Reviewing and approving batch records, logbooks, and quality documentation
Supporting deviations
Partnering cross-functionally with Manufacturing, QC, and Engineering teams
Identifying opportunities for continuous improvement and operational excellence
Acting as a quality advocate, promoting a culture of compliance and accountability

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans

Fulltime

Associate Quality Control

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , Thousand Oaks

Salary:

62571.90 - 84656.10 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 2 years of Quality experience OR Associate’s + 6 months of Quality experience OR Bachelor’s

Job Responsibility

Responsible for one or more of the following activities in QC: analytical testing, sample and data management and equipment maintenance
Perform routine laboratory procedures such as sample analysis, standard and solution preparation
Responsible for documenting, compiling, interpreting, reviewing and entering laboratory data
Providing and communicating results, maintaining/operating specialized equipment and drafting and revising documents such as Analytical Methods, SOPs and technical reports
Support introduction of new methods/techniques into the lab
Perform basic assay and instrument troubleshooting

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

Quality Assurance Senior Associate, Drug Substance Plant

In this role as Senior Associate QA, you will be responsible for providing quali...

Location

United States , Thousand Oaks

Salary:

86928.00 - 106536.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 4 years quality assurance work experience
Associate’s + 2 years quality assurance work experience
Bachelor’s + 6 months quality assurance work experience
Master's
Quality and manufacturing experience in biotech or pharmaceutical industry
Bachelor’s Degree in a Science Field
Ability to successfully manage workload to timelines
Familiarity with basic project management tools
Demonstrated ability to consistently deliver on-time, and high-quality results
Ability to operate in a matrixed or team environment

Job Responsibility

Provide daily guidance and support to Production staff on compliance with Standard Operating Procedures (SOPs) and Work Instructions
Maintain a strong presence in Drug Substance (DS) areas to oversee GMP operations and quality systems
Serve as the first point of contact for quality-related production queries during DS operations
Lead, mentor, and coach Operations and support personnel on quality matters, fostering a strong Quality culture at the site
Review and approve batch production records and other GMP documentation to support daily operations
Compile and review batch records for manufactured lots in preparation for batch disposition
Own, review, and approve controlled documents, including SOPs, Work Instructions, and Forms
Collaborate effectively within a team matrix environment
Work across a three shift rotation including night shift

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

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