Associate, Product (Labs) Job at Bully Pulpit International (Washington)

Drug Product Manufacturing Associate I

The Manufacturing Associate I is responsible for executing GMP production of inj...

Location

United States , San Diego

Salary:

21.98 - 25.64 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

High school diploma required
Bachelors in a science or engineering discipline preferred
Minimum of zero to two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions
Ability to follow instructions with direct supervision
Detail oriented with strong written and verbal communication skills
Demonstrated ability to follow detailed directions in a manufacturing GMP environment
Familiarity with cGMP, manufacturing, machine operations, and data entry
Must be familiar with Microsoft Office applications

Job Responsibility

Train in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility
Train on required SOP's and execute training curriculum
Prepare materials needed for aseptic operations
Performs various routine manufacturing tasks on complex equipment under the guidelines of established SOP’s and cGMP regulations
Accurately documents data and completes batch records as needed
Reliably executes well defined SOP’s
Operates in clean room environments in accordance with established policies and procedures
Collects and disposes of lab wastes according to established procedures
Regular and reliable attendance on a full time basis [or in accordance with posted schedule]
Embodies PCI Pharma Service’s cultural values and aligns daily actions with department goals and company culture

What we offer

Paid time off
Health insurance coverage (including dental and vision)
Flexible spending account
401(k) plan
Eligibility for an annual performance bonus

Fulltime

Drug Product Manufacturing Associate I

The Manufacturing Associate I is responsible for executing GMP production of inj...

Location

United States , San Diego

Salary:

21.98 - 25.65 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

High school diploma required
Bachelors in a science or engineering discipline preferred
Minimum of zero to two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions
Ability to follow instructions with direct supervision
Detail oriented with strong written and verbal communication skills
Demonstrated ability to follow detailed directions in a manufacturing GMP environment
Familiarity with cGMP, manufacturing, machine operations, and data entry
Must be familiar with Microsoft Office applications

Job Responsibility

Train in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility
Train on required SOP's and execute training curriculum
Prepare materials needed for aseptic operations
Performs various routine manufacturing tasks on complex equipment under the guidelines of established SOP’s and cGMP regulations
Accurately documents data and completes batch records as needed
Reliably executes well defined SOP’s
Operates in clean room environments in accordance with established policies and procedures
Collects and disposes of lab wastes according to established procedures
Regular and reliable attendance on a full time basis [or in accordance with posted schedule]
Embodies PCI Pharma Service’s cultural values and aligns daily actions with department goals and company culture

What we offer

Eligible for 10% pay differential
Paid time off
Health insurance coverage (including dental and vision)
Flexible spending account
401(k) plan
Eligibility for an annual performance bonus

Fulltime

Product Development Associate

We are looking for a freelance Product Development Associate for a top apparel c...

Location

United States , Los Angeles

Salary:

30.00 - 33.00 USD / Hour

Solomon Page

Expiration Date

Until further notice

Requirements

Minimum 3 years product development experience in retail or wholesale with overseas offices
High school degree
2 year college degree
BA or BS a preferred
Knowledge of technical design, fabric, yarns, knit and woven construction
Knowledge of print technique
Experience with duties and import limitations
Knowledge of time and action and production calendars

Job Responsibility

Negotiates appropriate costs and deliverables with sourcing partners to ensure best profit margin for the products are achieved
ensures tech pack turnovers to sourcing partners and factories
Manages production process from point of conception to finished product
Works closely with buyers and Product Development team to ensure buyer’s vision of product is achieved during the sourcing process
follows up with design team on technical design package and chart production flow
communicates with the vendors to make accurate counter samples
Obtains approvals for fabric, lab dip, and trims
Handles on-going communication with sourcing partners and resolves all production issues through teaming with appropriate business partners
Communicates with related business partners regarding product development progress to the assigned categories
alerts the partners of any unexpected issues and negotiates resolutions with factories

What we offer

medical
dental
401(k)
direct deposit
commuter benefits

Senior/Research Associate, Drug Product Development

We are seeking a skilled and motivated Senior/Research Associate to join our Del...

Location

United States , South San Francisco

Salary:

75000.00 - 100000.00 USD / Year

NewLimit

Expiration Date

Until further notice

Requirements

MS in Biomedical Engineering, Chemical Biology, Pharmaceutical Sciences, or a related discipline with 2+ years of industry experience or equivalent experience
Experience formulating LNPs with diverse lipid components for nucleic acid delivery
Experience with purification techniques, including dialysis, Tangential Flow Filtration (TFF), ultracentrifugation, and sterile filtration
Proficiency in LNP analysis using DLS, LC-UV, LC-CAD, CGE, fragment analyzers, Osmolality, MALS, ELISA, and fluorescence-based 96-well plate assays

Job Responsibility

Formulate, downstream process, and characterize LNPs for nucleic acid delivery across diverse model systems, including pre-clinical models
Partner with the Epigenetic Editing and Product teams (Immunology, Metabolism, Vascular) to meet LNP requirements for reprogramming interventions at both small and large scales
Develop and optimize LNP compositions, downstream processing and analytical methods to establish robust production protocols
Map future formulation needs, manage material procurement, and ensure the lab is equipped for upcoming programs
Interpret complex experimental data to drive decision-making within Delivery Science and Preclinical Development workstreams
Maintain rigorous and detailed records of experimental protocols and results in an Electronic Laboratory Notebook (ELN)

What we offer

Health, dental, and vision insurance
401(k) with company match
Paid parental leave
Industry-leading paid time off (PTO) — 20 days/year for all employees + holidays
Meals and snacks on-site

Fulltime

Associate QA Manager - Labs

Responsible for managing the plant Quality Assurance Soup Laboratories including...

Location

United States , Maxton

Salary:

90400.00 - 130000.00 USD / Year

THE VAIL CORPORATION

Expiration Date

Until further notice

Requirements

High School Diploma or GED
3+ years of Quality Assurance, Laboratory practices or Food experience within a manufacturing environment

Job Responsibility

Managing the plant Quality Assurance Soup Laboratories including Chemistry Lab and Microbiological Lab
Coordinating releases of products, startups of new and reformulated products, supplier and incoming materials COA's, and Noncompliance's
Managing laboratory data and coordinate resolution of specification issues with materials and products
Coordinating test runs, new product/reformulations start-ups with Product Development, Quality System and plant operations management
Reporting outcome of start-ups and reformulations to management
Organizing and reporting on conformance of new product to specifications
Coordinating corrective action plans
Establishing schedule and ensuring sampling of products per specification and Food Safety/Quality requirements
Ensuring Microbiology and chemistry lab compliance with corporate requirements
Ensuring data base and MES system maintenance

What we offer

Medical
Dental
Short and long-term disability
AD&D
Life insurance
Matching 401(k) plan with immediate vesting
Unlimited sick time
Paid time off
Holiday pay
Employee Resource Groups (ERGs)

Fulltime

Research Associate I - R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master in Pharmacy or equivalent discipline with 6 to 10 years of experience
PhD in biophysics, biochemistry or equivalent discipline with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions
Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
To verify the shelf life of the chemical or reagent before performing analysis of the material or product
To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Research Associate I - R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions is mandatory
Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
Traveling to external facilities, as and when required, is a mandatory requirement for this position
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
Data recording in ELN and sign off must be completed on time

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Research Associate I - R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Masters (Pharmacy, or equivalent discipline) with 6 to 10 years of experience, or, PhD (biophysics, biochemistry or equivalent discipline) with 0 to 5 years of experience with spectroscopic and biophysical methods, including CD, FTIR, fluorescence spectroscopy
Competency in the acquisition, processing and data analysis by CD, FTIR, and fluorescence spectroscopy for analysis of proteins and peptides for regulatory submissions is mandatory
Expertise in computational chemistry, molecular modeling and statistical methods are beneficial attributes
Basic understanding of working principles of liquid chromatographic methods, dynamic light scattering, AF4-MALS, SV-AUC, & related orthogonal methods to assess protein higher order structures
Proficiency in literature search through publication and patent databases, repositories (e.g. Pubmed), scientific webinars by regulatory agencies, etc, to remain updated on advanced characterization methods and recent scientific developments
Knowledge of pharmacopoeia, ICH Guidelines and means to implement them for product development
Experience in the operation, calibration and preventive maintenance of NMR and other instruments to ensure continued usage
Trouble shooting of various problems obtain during the product development
Knowledge of good laboratory practices and good documentation practices
Communication skills

Job Responsibility

To perform advanced characterization of complex injectable drugs, including proteins & peptides, oligonucleotides, iron formulations, carbohydrates & other biomolecular APIs and various impurities in lyophilized, liquid, emulsions & other formulations for regulatory submission following GLP norms
To manage outsourced studies at CROs, academic institutes & other external facilities, from study design, execution, analysis and report preparation
To demonstrate subject matter expertise and help overcome technical challenges in product development, by liaising with formulation and other cross-functional teams as a Subject Matter Expertise (SME)
To understand the project with guidance of Sub-department Manager and follow their instructions
To provide necessary assistance for various procurement activities, review quotations, engage suppliers to procure required goods & services in a timebound manner
To complete the planned work in the stipulated time frame, inform the Sub-department Manager if any deviation or issues are observed
To keep track of each activity related to product analysis and development activities
To carry out all the testing and data recording according to the approved SOPs/ ALCOA++ principle and current pharmacopoeia
To verify the shelf life of the chemical or reagent before performing analysis of the material or product
To follow Good Documentation Practices & Good Laboratory Practices, maintain lab notebooks & other records appropriately

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

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Associate, Product (Labs)

Job Description

Job Responsibility

Requirements

What we offer

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