For Us, It&#**Apply on the website**;s A Mission At Mylan, we mean it
when we say we work every day to provide access to high quality
medicines to the world&#**Apply on the website**;s 7 billion people.
If you are unconventional, relentless and passionate. If you believe
in doing what&#**Apply on the website**;s right, not what&#**Apply on
the website**;s easy. If you are a doer and have a passion for serving
others, we want to talk to you. MAKE A DIFFERENCE At Mylan, each
person has the ability to make a difference. From the providers who
sell and market our products, to the producers who develop and
manufacture them and finally to our business partners who support the
providers and producers, we all have a mission critical role.
Here&#**Apply on the website**;s how this role will help:
* Process Validation/Qualification projects will be across a range of
production areas which may include Process, Cleaning, Software,
Utility and Facility projects.
* Generation, execution and close out of validation projects
relating to existing products and new product introductions.
* Accountable for writing, executing & reporting of all validation
activities including but not limited to (FAT / IQ / OQ / PQ / FMEA
Risk Assessments/ PVP).
* Participate in project teams and assist in determining project
schedules and the appropriate levels of validation.
* Execution and documenting risk assessments (FMEA) with respect to
validation activities.
* Perform validation functional testing as required. Track and
resolve deviations during qualification activities.
MAKE OUR VALUES YOUR VALUES
Mylan hires only the best. People who thrive in a culture of
innovation and empowerment. People who are active learners and have a
positive attitude. People who are leaders and know that by working
together we can run faster, reach higher and achieve more. By doing
so, we will continue to set new standards in health care. Here are the
minimum qualifications and essential functions for this position:
* Bachelor&#**Apply on the website**;s degree in Science,
Engineering, Technology or a related discipline.
* Minimum of 3 years? experience as a validation
engineer/specialist in a cGMP environment, preferably in an oral solid
dose facility.
* Full understanding of cGMP requirements including Annex **Apply on
the website** and Annex **Apply on the website**.
* Effective technical writing skills.
* Excellent interpersonal, leadership, communication (written and
verbal) and time-management skills are essential.
* Must be flexible and able to manage multiple priorities
simultaneously.
* Must take ownership of all task assigned and proactively see them
through to conclusion
Location: Sutton
For Us, It&#**Apply on the website**;s A Mission At Mylan, we mean it
when we say we work every day to provide access to high quality
medicines to the world&#**Apply on the website**;s 7 billion people.
If you are unconventional, relentless and passionate. If you believe
in doing what&#**Apply on the website**;s right, not what&#**Apply on
the website**;s easy. If you are a doer and have a passion for serving
others, we want to talk to you. MAKE A DIFFERENCE At Mylan, each
person has the ability to make a difference. From the providers who
sell and market our products, to the producers who develop and
manufacture them and finally to our business partners who support the
providers and producers, we all have a mission critical role.
Here&#**Apply on the website**;s how this role will help:
* Process Validation/Qualification projects will be across a range of
production areas which may include Process, Cleaning, Software,
Utility and Facility projects.
* Generation, execution and close out of validation projects
relating to existing products and new product introductions.
* Accountable for writing, executing & reporting of all validation
activities including but not limited to (FAT / IQ / OQ / PQ / FMEA
Risk Assessments/ PVP).
* Participate in project teams and assist in determining project
schedules and the appropriate levels of validation.
* Execution and documenting risk assessments (FMEA) with respect to
validation activities.
* Perform validation functional testing as required. Track and
resolve deviations during qualification activities.
MAKE OUR VALUES YOUR VALUES
Mylan hires only the best. People who thrive in a culture of
innovation and empowerment. People who are active learners and have a
positive attitude. People who are leaders and know that by working
together we can run faster, reach higher and achieve more. By doing
so, we will continue to set new standards in health care. Here are the
minimum qualifications and essential functions for this position:
* Bachelor&#**Apply on the website**;s degree in Science,
Engineering, Technology or a related discipline.
* Minimum of 3 years? experience as a validation
engineer/specialist in a cGMP environment, preferably in an oral solid
dose facility.
* Full understanding of cGMP requirements including Annex **Apply on
the website** and Annex **Apply on the website**.
* Effective technical writing skills.
* Excellent interpersonal, leadership, communication (written and
verbal) and time-management skills are essential.
* Must be flexible and able to manage multiple priorities
simultaneously.
* Must take ownership of all task assigned and proactively see them
through to conclusion
We need : English (Good)
Type: Permanent
Payment:
Category: Others
