Technical Officer Clinical Biology Job at Randstad (Melbourne, Bundoora West)

Process Validation Associate

This position reports to the Process Validation Manager and is responsible for m...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor of Arts/Sciences (BA/BS) degree, or higher, in a technical discipline (physical, engineering, chemical or biological sciences) is required
8+ years experience in a cGMP regulated manufacturing environment, with exhibited knowledge or proficiency in process validation, process sciences and change control
Organizational and management skills to participate in multi-discipline project groups
Ability to communicate with, present data to, and defend approaches in front of variable hierarchical audiences, scientific disciplines and health authority reviewers/inspectorate
Ability to comprehend scientific/technical information related to equipment, processes, and regulatory expectations
Understanding and demonstrated knowledge of regulatory requirements, guidelines, and recommendations for process validation expectations
Proficiency with technical writing expected
Proficiency with standard office software applications, including MS Word, MS Excel, MS Project, MS Power Point

Job Responsibility

Perform process validation activities related to BioMarin’s drug substance and drug products, through defined clinical and commercial stages
Execute (protocol generation, execution, and final package preparation) process validation activities related to the implementation of process changes and new processes
Assist with preparation of regulatory filings, with answering questions from regulatory agencies, and with presentations of materials during regulatory inspections/partner audits
Development and implementation of SOPs/Guideline documents with systemic procedural improvements
Determine methods and procedures on new assignments with supervision and in accordance with developed practices and procedures
May participate on sub-teams
Gain/maintain knowledge of industry standards and regulatory requirements for products developed and manufactured by BioMarin, validation techniques/approaches and systems utilized at BioMarin
Participate in multi-departmental meetings & project teams
Identifies and assists with implementation of improvements to Process Validation systems (department level impact)
Generation of process validation master plans, core validation master plans and additional supporting documentation

Fulltime

Lab Supervisor - Microbiology

Are you an experienced clinical laboratory professional looking for leadership o...

Location

United States of America , Tampa

Salary:

Not provided

Labcorp

Expiration Date

Until further notice

Requirements

Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or a non-traditional Associate’s degree that meets local regulatory
Minimum 5 years of experience as a Technologist/Technician
FL State Clinical Laboratory Supervisor license required
Strong working knowledge of CLIA, CAP and relevant state regulations
Understanding of laboratory operations as well as policies and procedures
Proficient with Laboratory Information Systems and Microsoft Office
Strong communication skills
both written and verbal
High level of attention to detail with strong organizational skills
Comfortability making decisions in a changing environment

Job Responsibility

Supervise the day to day operations of the Microbiology department
Ensure laboratory tests are accurately performed and results are reported in a timely manner
Directly supervise, train, and mentor laboratory personnel of the department
Monitor daily workflow in the lab and schedule adequate assay coverage
Responsible for ensuring all shifts in the department are properly staffed
Research and resolve any production errors while escalating when necessary
Engage in continuous process and service level improvements
Ensure all equipment is being properly maintained through Quality Control
Prepare and maintain Quality Assurance records and documents
Evaluate new process improvements and make appropriate recommendations

What we offer

$10,000 sign on bonus
Medical
Dental
Vision
Life
STD/LTD
401(k)
Paid Time Off (PTO) or Flexible Time Off (FTO)
Tuition Reimbursement
Employee Stock Purchase Plan

Fulltime

Molecular Technologist II

The 2nd Shift Molecular Technologist II (Sat - Tues 2:00pm - 12:30am) is respons...

Location

United States , Phoenix

Salary:

57000.00 - 102000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in a chemical, biological or clinical laboratory science or medical technology
2+ years of pertinent clinical laboratory experience
Working knowledge of laboratory concepts and applications as well as laboratory safety and regulatory requirements
Technically proficient in basic molecular or microbiology techniques and related equipment
Proficient in Microsoft Office programs, such as Word, Excel, and PowerPoint
Authorization to work in the United States without sponsorship
Demonstrated ability to perform the Essential Duties of the position with or without accommodation

Job Responsibility

Perform processing of patient samples using molecular biology protocols governed by standard operating procedures (SOPs)
Extract nucleic acids from sample types
including, but not limited to, human tissue, blood, and saliva
Construct DNA/RNA libraries and NGS
Operate liquid handling robots
Analyze and problem solve moderate sample and/or plate issues
Review patient and control data, and document according to laboratory quality procedures
Maintain sufficient inventory of laboratory supplies for daily operations
Contribute to training efforts
provide and create training materials

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Manager, Process Development and Automation

The Manager, Process Development and Automation provides leadership support to t...

Location

United States , Redwood City

Salary:

124000.00 - 200000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Engineering, Technology, Molecular Biology, Clinical Laboratory science, Chemical, biological, Electronics, or related field and 2 years’ experience as outlined in the essential duties
or Associates Degree in a Microbiology field or Engineering Science and 4 years’ experience as outlined in the essential duties in lieu of Bachelor's degree
2+ years in a role with progressively increasing responsibilities such as laboratory management, quality and control, lead technologist, or technical specialist
8+ years’ experience in process development, laboratory automation, service engineering, laboratory setting, or related industry as outlined in the essential duties
Successful track record of leading projects holistically from inception to successful implementation with cross-functional participation in a matrixed environment
Proficient in computer aided design software (SolidWorks) or statistical analysis programs (JMP), Microsoft Office Word, Excel, PowerPoint, and similar software
Working knowledge of regulatory requirements to make sure the laboratory is in compliance with all applicable laws and regulations, including applicable CLIA, CAP, California, New York (CLEP), and other requirements
Experience in the design, development, and implementation of solutions comprised of integrated automated and manual workflows, including software components in a highly regulated environment (ISO 13485 or 21 CFR Part 820, or cGMP using 21 CFR Part 210, 21 CFR Part 211)
Understanding and application of user requirements, system requirements, risk assessments, trace matrices, FMEA, etc. translating into a successful track record in understanding complex end-user applications, collecting and clearly documenting end-user needs, and translating those into clear, concise, and testable requirements
1+ years in a leadership role with staff and team accountability

Job Responsibility

Provide leadership on best practices for the development of processes and products in a regulated environment
Lead the team in continuous improvement projects and support other areas’ needs dependent on demand
Coach, mentor, and raise the team's ability to deliver and exceed expectations while creating opportunities for team member development
Consistent demonstration of exceptional leadership qualities
Effectively manage, support, and guide your team
Serve as a resource for employees by sharing and knowledge transfer of best practices for experiment design and execution
Ensure that any incoming support requests from outside of the normal channels are properly routed
Ensure that assigned support requests from cross-functional project teams or business units are being actively addressed
Assist and coordinate training methodology and training documentation in conjunction with other leadership
Provide mentoring and technical guidance to PDA engineers and scientists

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Lead Technical Services Application Scientist

The Lead Application Scientist, Technical Services will provide outstanding tech...

Location

United States , Madison

Salary:

84000.00 - 150000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Life Sciences or field as outlined in the essential duties
10+ years of experience in the life sciences industry
5+ years of experience working in a molecular diagnostic or clinical laboratory
5+ years of experience working in next generation sequencing
Demonstrated advanced proficiency or coursework with molecular biology techniques and Real-Time- polymerase chain reaction (PCR) Assays
Demonstrated advanced knowledge of clinical lab regulations for computer aided planning (CAP), clinical laboratory improvement amendments (CLIA), invitro diagnostic regulation (IVDR), and food and drug administration (FDA)
Demonstrated understanding of statistical and mathematical methods in biology or genetics
Advanced data analysis skills and analytical aptitude
Proficiency in Microsoft Office programs, such as Word, Excel, PowerPoint, Outlook, Access, and OneNote
Demonstrated ability to perform the essential duties of the position with or without accommodation

Job Responsibility

Receive and document incoming customer communications
Work cooperatively with the technical services team and internal functional departments to troubleshoot and resolve customer questions or requests related to reagents, consumables, and assay issues
Lead troubleshooting of customer issues through root cause investigation, experiment design, study execution, data analysis, and reporting
Conduct bench level experiments within several product areas
Prepare technical experiment reports with all technical specifications and information to present to the supervisor or project team
Lead development of training materials for internal and external customers and train customers
Coordinate with the development and marketing teams for proper implementation of new products to provide technical input and participate in decisions affecting project plans and experimental design
Prepare detailed technical protocols
Communicate the customer feedback for product requirements to the development team for better designs and implementation of new and existing products
Identify gaps in processes, make recommendations, and implement change

What we offer

Paid time off (including days for vacation, holidays, volunteering, and personal time)
Paid leave for parents and caregivers
A retirement savings plan
Wellness support
Health benefits including medical, prescription drug, dental, and vision coverage
Bonus eligibility

Fulltime

Pre-Analytical Clinical Laboratory Trainer

The Clinical Laboratory Trainer prepares and facilitates training for new hire a...

Location

United States , Phoenix

Salary:

74000.00 - 122000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Associates Degree in Business Administration, Education, Chemical, Physical, Biological, or Clinical Laboratory Science, Medical Technology, or field related to the essential duties of the job
or High School Diploma/General Education Degree (GED) and 2 years of relevant experience in lieu of Associates Degree
4+ years of professional experience related to the essential duties of the position
1+ years of clinical laboratory experience with a strong understanding of working in a laboratory with professional working knowledge of HIPAA, GLP, GDP, and laboratory terminology and equipment
Strong understanding of instructor-led, virtual-led, technical, and/or hands-on/on-the-job training
Excellent computer skills to include Internet navigation, use of virtual meeting tools and platforms, email usage, word processing, and data/records management
Proficient in Microsoft Office programs, such as: Word, Excel, PowerPoint, Outlook, or OneNote
Demonstrated ability to perform the essential duties of the position with or without accommodation
Authorization to work in the United States without sponsorship

Job Responsibility

Delivers training through in-person training, virtual training, hands-on/on-the-job training, virtual training, and other modalities, as needed
Identifies and adapt training/facilitation style to meet learner needs, in the moment
Facilitates small or large group learning sessions
Administers learning exams and/or competency direct observations
Assists in creation, edit, and maintenance of training and competency materials
Maintains competency in assigned test processes, in accordance with regulatory requirements
Performs pre-analytic, analytical, and/or post-analytical tasks, in the laboratories, as assigned
Stays informed and up to date on new/edited SOPs, assignments, and changes in the laboratory processes in which they train
Participate in team projects, as assigned
Evaluates the effectiveness of training through surveys, observations, and feedback

What we offer

paid time off (including days for vacation, holidays, volunteering, and personal time)
paid leave for parents and caregivers
a retirement savings plan
wellness support
health benefits including medical, prescription drug, dental, and vision coverage
bonus eligibility

Fulltime

New

Clinical Lab Team Lead - Blood Bank

Are you an experienced clinical laboratory professional looking for leadership o...

Location

United States of America , Nashville

Salary:

Not provided

Labcorp

Expiration Date

Until further notice

Requirements

Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or a non-traditional Associate’s degree that meets local regulatory
Minimum 3 years of experience as a Technologist/Technician required
Blood bank experience highly preferred
ASCP and/or AMT Certifications are preferred
Prior supervisory or leadership experience is a plus
Understanding of laboratory operations as well as policies and procedure
Proficient with Laboratory Information Systems and Microsoft Office
Strong communication skills
both written and verbal
High level of attention to detail with strong organizational skills

Job Responsibility

Assist the supervisor with the day to day operations of the Blood Bank
Send daily, weekly and monthly productions reports to management
Assist with the training of new hires and the development of current employees
Keep supervisor informed of group progress, problems, employee performance and any significant factors affecting assigned responsibilities
Determine the acceptability of specimens for testing according to established criteria
Perform routine and complex technical procedures and functions according to SOPs
Monitor, operate and troubleshoot instrumentation to ensure proper functionality
Prepare, test and evaluate new reagents or controls
Report accurate and timely test results in order to deliver quality patient care
Perform and document preventive maintenance and quality control procedures

What we offer

$10,000.00 SIGN ON BONUS (External Candidates Only)
Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan

Fulltime

Area Business Manager, Allergy/ENT

The Area Business Manager (ABM) is responsible for engaging Allergists and ENTs,...

Location

United States , San Diego

Salary:

125250.00 - 180916.66 USD / Year

Sanofi-Aventis Deutschland GmbH

Expiration Date

May 31, 2026

Requirements

Bachelor’s degree from an accredited four-year college or university
Minimum 3 years of pharmaceutical, medical device or biotech Sales experience, OR relevant clinical experience and/or in a Sanofi development program
Demonstrated ability to learn and apply technical and scientific product-related information
Ability to travel to meetings/trainings/programs as necessary - additional travel may be required within the assigned territory
Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines
Ability to operate as a “team player” in cooperation with collaboration partners and internal colleagues to reach common goals
Valid Driver’s License

Job Responsibility

Engage Allergy/Immunology/ENT customers within assigned geographical territory and deliver clinically focused message to introduce, launch, grow brand-share and revenue and to consistently deliver on product goals for asthma, CRSwNP, atopic dermatitis, CSU and EOE indications
Collaborate and coordinate with other key field-based stakeholders such as Regeneron Sales Professional counterparts, Medical Science Liaisons, Field Reimbursement and Market Access teammates, Thought Leader Liaisons, and others in their territory to proactively address customer needs, identify market dynamics and trends, develop strategies which support brand and corporate objectives, and ensure optimal account success within their assigned geography
Develop strong working relationships with immunology experts and all additional Allergy/ENT specialists in assigned geography as well as biologic coordinators, office staff and other important health care personnel and key patient advocacy support groups as directed
Drive results by identifying key opportunities and developing strategic business plans to generate product utilization and grow territory business
Plan, organize, and execute local promotional speaker programs and activities. Maximize budget allocated to the geographic territory to support execution of strategies and tactics and generate/grow the business
Participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences)
Own business opportunities within respective geographic area, which includes coordination and calling upon large group practices and other key targets to drive overall product results
Establish relationship with thought leaders in assigned territory. Primary objective is to drive industry leading customer value

What we offer

high-quality healthcare, prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave

Fulltime

Technical Officer Clinical Biology

Randstad

Location:
Australia , Melbourne, Bundoora West

Category:
Education

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 08, 2026

Expiration:
March 28, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Technical Officer Clinical Biology

Randstad

Location:Australia , Melbourne, Bundoora West

Category:Education

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:March 08, 2026

Expiration:March 28, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Location:
Australia , Melbourne, Bundoora West

Category:
Education

Contract Type:
Not provided

Job Posted:
March 08, 2026

Expiration:
March 28, 2026