Biology Expert Job at Handshake

New

Secondary Science Teacher

Are you a scientific thinker with a passion for inspiring the next generation? W...

Location

United Kingdom , Banstead

Salary:

140.00 - 233.00 GBP / Day

Randstad

Expiration Date

August 13, 2026

Requirements

Hold Qualified Teacher Status (QTS) or equivalent
ECTs are highly encouraged to apply.
Possess a degree in a Science-related field with a comprehensive understanding of the National Curriculum.
Demonstrate excellent communication skills and the ability to build rapport with students quickly.
Possess an enhanced DBS on the update service, or the willingness to apply for one, with a firm commitment to safeguarding.

Job Responsibility

Facilitate engaging lessons across Key Stage 3 and Key Stage 4, bringing subjects like Biology, Chemistry, and Physics to life.
Provide expert instruction, focusing on core curriculum mastery, data analysis, and scientific inquiry.
Support examination cohorts with targeted preparation for GCSE and A-Level success.
Maintain a safe, structured, and disciplined laboratory environment, ensuring all health and safety protocols are strictly observed.
Adapt teaching methods to support students with diverse learning needs, including SEND and EAL, to ensure accessibility for all.

What we offer

Flexible, term-time employment options suitable for your work-life balance.
Competitive daily rates (£140 - £233) with weekly pay.
The opportunity to experience diverse school environments and departmental cultures.
training and education
Safeguarding & Prevent

Fulltime

Sr Mgr, Regulatory Affairs

A Senior Manager of Global Regulatory Affairs leads the development and executio...

Location

United States , Deerfield

Salary:

152000.00 - 209000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree or country equivalent in a scientific discipline
Master's and/or PhD will be preferred
Minimum of 7-year experience in RA
Expert Regulatory knowledge
Sound basis of Scientific knowledge
Management skills
Ability to oversee multiple projects in a matrix team environment
Excellent oral and written communication and presentation skills
Demonstrated excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities
Technical and management skills

Job Responsibility

Serves as the Global Regulatory Lead for Baxter's hemostat and sealant product(s)
Provide technical and strategic input for regulatory decisions
Identify & prioritize key areas of risk
Monitor, evaluate, and interpret all applicable regulatory requirements
Assess impact of new regulations
Evaluate technical and scientific information
Act as primary contact for meetings with regulatory authorities
Maintain appropriate communication within the RA function
Plan and manage complex projects
Initiate, manage and maintain operational activities

What we offer

Medical and dental coverage starting day one
Basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

Sr Mgr, Regulatory Affairs

A Senior Manager of Global Regulatory Affairs leads the development and executio...

Location

United States , Deerfield

Salary:

152000.00 - 209000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree or country equivalent in a scientific discipline
Master's and/or PhD will be preferred
Minimum of 7-year experience in RA
Expert Regulatory knowledge
Sound basis of Scientific (Training/ Communications) knowledge
Management skills
Ability to oversee multiple projects in a matrix team environment
Excellent oral and written communication and presentation skills
Demonstrated excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities
Technical and management skills

Job Responsibility

Serves as the Global Regulatory Lead for Baxter’s hemostat and sealant product(s) registered as biologic/combination products
Provide technical and strategic input for regulatory decisions aligned with business strategy
Identify & prioritize key areas of risk and probability of occurrence as well as ensure implementation of mitigation plans and follow ups
Monitor, evaluate, and interpret all applicable regulatory requirements, assure compliance with Baxter and external standards
Assess impact of new regulations and provide feedback
Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks
Act as primary contact for meetings with regulatory authorities including planning and leadership
Maintain appropriate communication within the RA function, with Global Marketing, and with other functions primarily at the project team level
Plan and manage complex projects and prioritize workload
Initiate, manage and maintain operational activities in support of new and existing marketing authorizations

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

Senior Director, Quality Assurance

Theradaptive is revolutionizing the field of therapeutic delivery with a pipelin...

Location

United States , Frederick

Salary:

Not provided

Theradaptive

Expiration Date

Until further notice

Requirements

Bachelor's degree (required) in Life Sciences, Biomedical Engineering, Chemistry, Biochemistry, or a related field
Advanced degree (M.S., Ph.D., or M.D.) strongly preferred
15+ years of progressive quality experience in the biopharmaceutical, biotech, or medtech industry, with at least 5 years in a senior leadership role (Director level or above)
Demonstrated experience with combination products, including working knowledge of both drug/biologic and device QMS frameworks
Direct experience managing FDA inspections (PAI, cGMP, QSR) and responding to 483 observations and Warning Letters
Hands-on experience with protein biologics or growth factors (e.g., rhPDGF, BMP, FGF, EGF, VEGF) in a GMP manufacturing or quality context
Experience with sterile or aseptic combination products is highly preferred
Expert-level knowledge of: 21 CFR Parts 210/211 (Drug cGMP), 21 CFR Part 820 / ISO 13485 (Device QMS), 21 CFR Part 4 (Combination Products)
Expert-level knowledge of: ICH Q7, Q8, Q9, Q10, Q11 guidelines
Expert-level knowledge of: ISO 14971 (Risk Management), ISO 10993 (Biocompatibility)

Job Responsibility

Design, implement, and own an integrated QMS that satisfies 21 CFR Parts 210/211 (drug/biologic GMP), 21 CFR Part 820 / ISO 13485:2016 (medical device QMS), and ICH guidelines (Q7, Q8, Q9, Q10)
Ensure the QMS addresses the regulatory designation of the combination product (PMOA-based lead center: CDRH or CDER) and the requirements of the non-lead center
Develop and maintain all quality policies, SOPs, work instructions, and quality plans across the product lifecycle
Drive QMS digital transformation initiatives, including electronic quality management platforms (e.g., Veeva Vault QMS, MasterControl, TrackWise)
Serve as the company's subject-matter expert on 21 CFR Part 3 (combination product designation), 21 CFR Part 4 (regulation of combination products), and applicable guidance documents
Lead cross-functional efforts to align quality requirements for both the protein growth factor drug/biologic constituent and the device constituent part throughout CMC development, scale-up, and commercialization
Oversee the integration of device design controls (21 CFR 820.30) with drug development quality requirements, ensuring alignment in risk management activities per ISO 14971
Collaborate closely with Regulatory Affairs on BLA, PMA, 510(k), or De Novo submission strategies — specifically quality module content (Module 3 / CTD, Design History File, Device Master Record)
Prepare and lead quality-related FDA interactions including pre-submission meetings, Agency responses, and inspection readiness activities
Support compliance with EU MDR 2017/745, IVDR, and country-specific registration requirements for international expansion

Sr Mgr, Regulatory Affairs

A Senior Manager of Global Regulatory Affairs leads the development and executio...

Location

United States , Deerfield

Salary:

152000.00 - 209000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree or country equivalent in a scientific discipline
Master's and/or PhD will be preferred
Minimum of 7-year experience in RA
Expert Regulatory knowledge
Sound basis of Scientific (Training/ Communications) knowledge
Management skills
Ability to oversee multiple projects in a matrix team environment
Excellent oral and written communication and presentation skills
Demonstrated excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities
Technical and management skills

Job Responsibility

Serves as the Global Regulatory Lead for Baxter's hemostat and sealant product(s) registered as biologic/combination products
Provide technical and strategic input for regulatory decisions aligned with business strategy
Identify & prioritize key areas of risk and probability of occurrence as well as ensure implementation of mitigation plans and follow ups
Monitor, evaluate, and interpret all applicable regulatory requirements, assure compliance with Baxter and external standards
Assess impact of new regulations and provide feedback
Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks
Act as primary contact for meetings with regulatory authorities including planning and leadership
Maintain appropriate communication within the RA function, with Global Marketing, and with other functions primarily at the project team level
Plan and manage complex projects and prioritize workload
Initiate, manage and maintain operational activities in support of new and existing marketing authorizations

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

New

Medical Technologist III - Anatomic Pathology and Histology

Location

Japan , Saitama

Salary:

Not provided

Labcorp

Expiration Date

Until further notice

Requirements

Bachelor's degree in biological, chemical, physical, agricultural or pharmaceutical sciences
Proficiency in English and Japanese

Job Responsibility

Demonstrates thorough working knowledge of instruments/equipment in the department
Able to provide troubleshooting guidance to staff to resolve complex instrument and equipment problems
Coordinates the timely development and completion of training materials and checklists
Seeks and promotes expertise in department and across sites to ensure a consistent approach to training
Initiates revisions to SOPs or write new SOPs to reflect current processes that ensure compliance
Coordinates with other departments and other sites to ensure timely completion of SOP
Responsible for coordinating with other resources to ensure timely completion and implementation of new assay validations
May be asked to research, develop, validate and maintain procedures in area of responsibility and make recommendations on modification/improvement of procedures to management
Able to analyze existing processes and create new approaches or ideas to improve
Demonstrates extensive knowledge of all department functions, and may serve as subject matter expert for department on company wide initiatives

Fulltime

New

Secondary Science Teacher

Secondary Science Teacher | Subject Specialist | Local Secondary Schools Positi...

Location

United Kingdom , Bristol

Salary:

140.00 - 233.00 GBP / Day

Randstad

Expiration Date

August 08, 2026

Requirements

Hold QTS: You have Qualified Teacher Status (QTS) or an equivalent recognised teaching qualification (ECTs are highly encouraged to apply)
Are a Science Specialist: You have a degree in a Science-related field (Biology, Chemistry, Physics, or Combined Science), with a solid grasp of the KS3/KS4 National Curriculum
Are an Engaging Communicator: You can build rapport with teenagers quickly and use your passion for discovery to spark their interest in STEM
Are Committed: You hold an enhanced DBS on the update service (or are willing to apply) and are 100% dedicated to Safeguarding

Job Responsibility

Expert Lesson Delivery: Facilitate engaging demonstrations and theory-based lessons, encouraging students to think critically about evidence, variables, and global scientific challenges
GCSE & A-Level Focus: Support examination cohorts with targeted preparation, focusing on required practicals, data analysis, and the application of scientific mathematical skills
Classroom & Lab Safety: Maintain a disciplined and safe learning environment, ensuring all students follow laboratory protocols while engaging in curiosity-driven learning
Adaptive Support: Differentiate complex concepts on the fly to support students with SEND or EAL, ensuring that the Big Ideas of science are accessible to every learner

What we offer

Referral Bonus
PAYE
Weekly Pay

New

Secondary Science Teacher

Secondary Science Teacher | Subject Specialist | Local Secondary Schools Positi...

Location

United Kingdom , Bristol

Salary:

140.00 - 233.00 GBP / Day

Randstad

Expiration Date

August 08, 2026

Requirements

Hold QTS: You have Qualified Teacher Status (QTS) or an equivalent recognised teaching qualification (ECTs are highly encouraged to apply)
Are a Science Specialist: You have a degree in a Science-related field (Biology, Chemistry, Physics, or Combined Science), with a solid grasp of the KS3/KS4 National Curriculum
Are an Engaging Communicator: You can build rapport with teenagers quickly and use your passion for discovery to spark their interest in STEM
Are Committed: You hold an enhanced DBS on the update service (or are willing to apply) and are 100% dedicated to Safeguarding

Job Responsibility

Expert Lesson Delivery: Facilitate engaging demonstrations and theory-based lessons, encouraging students to think critically about evidence, variables, and global scientific challenges
GCSE & A-Level Focus: Support examination cohorts with targeted preparation, focusing on required practicals, data analysis, and the application of scientific mathematical skills
Classroom & Lab Safety: Maintain a disciplined and safe learning environment, ensuring all students follow laboratory protocols while engaging in curiosity-driven learning
Adaptive Support: Differentiate complex concepts on the fly to support students with SEND or EAL, ensuring that the "Big Ideas" of science are accessible to every learner

What we offer

training and education
PAYE
Referral Bonus
Weekly Pay

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Biology Expert

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Biology Expert

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