Commercial Laboratory Director

Commercial Laboratory Director
Company:

Glaxosmithkline


Details of the offer

Site Name:

Upper Merion, Belgium-Wavre, UK - Hertfordshire - Stevenage, UK - London, USA - Pennsylvania - Philadelphia
Posted Date:

Jun 24 2024
If you are an

employee potentially impacted and at risk of redundancy, please add the following statement at the top of your CV: "At Risk of Redundancy".
The

Commercial Laboratory Director

is accountable for

managing relationships with external analytical service providers as well as supporting the individual projects at those providers

.

The role will work in close partnership with

Global Supply Chain,

matrix project workstreams, budget holders, and R&D

to support analytical transfer from internal to external nodes and vice

-

versa

.

In addition,

this role

will support laboratory incident reports and deviations linked to

QC testing, for example out of specifications (OOS).
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
Manage the analytical supplier relationships and oversee execution of analytical deliverables

with contract laboratorie

s

from clinical to

commercial
Build relationships with analytical suppliers to deploy GSK common

objectives

and to ensure

contract laboratories

delivers to GSK standards, supplier

maintains

compliance with GMP requirements, and risks introduced to GSK network from use of supplier are

properly managed

and

mitigated
Continuously drive and deliver improvement across service, quality, safety, and cost which may include remediation, as needed with analytical suppliers to ensure compliance and viability of products for the long

term
Coordinate activities in matrix working environment to ensure products tested right first time, meet GSK standards

with competitive

pricing
Manage and support assessments necessary to develop analytical sourcing and supply chain recommendations (e.g., RFPs, make vs. buy)
Coordinate and implement finance standard work processes

and

ensure invoices from third-party CROs are reviewed on a monthly cadence and invoices will be

submitted

right first time.
Provide technical, compliance, and project management oversight for contract testing laboratories through technical site visits, data review, and monitoring of key performance indicators

.
Support digitalization and automation initiatives of metrics and data review
Accountable for generation and management of specifications and specification templates.
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
Bachelor's degree
5+ years'

experience in QC analytical labs management including oversight of contract analytical testing and implementation of digitalization and automation technologies in QC labs.
5+ years' experience in leadership
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
Master's Degree
Demonstrated knowledge of regulated environment

with e

xtensive knowledge of GMPs

, and

of

quality and

regulatory compliance requirements

for the

analytical testing of products from

development

to

commercialization.
Strategic quality technical expert that can engage and define analytical strategies across multiple functions.
Effectively coordinates

and build long-term

external collaborations with

third

parties.
Applies technical knowledge to form new ideas, anticipates and recognizes potential problems whilst providing workable solutions and can draw sound conclusions based on complex information or expertise from multiple specialty areas.
Provide analytical information to support the project team decision making process.
Ensures change management is followed for analytical methods and specifications.
Able to interact with peers,

subordinate

, and senior personnel in multidisciplinary

environment.
Demonstrated competency in project management
Excellent written/verbal communication, presentation and effective influencing skills
Works well as part of matrix teams
Please visit

GSK US Benefits Summary

to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at ******** (US Toll Free) or +******** (outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting

For the Record

site.

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Source: Grabsjobs_Co

Job Function:

Requirements

Commercial Laboratory Director
Company:

Glaxosmithkline


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